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Gingival overgrowth in fixed orthodontic therapy.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.22
Alina Cristina Rădeanu, Ilona Mihaela Liliac, Maria Cristina Munteanu, Mihai Surpăţeanu, Ciprian Laurenţiu Pătru, Elena Cristina Andrei

The oral mucosa can suffer a series of traumatic injuries from various causes (bacterial plaque, tartar, fillings, incorrectly adapted prosthesis). A risk factor generating periodontal diseases is represented by fixed orthodontic therapy, if the forces exerted on it are excessive. These forces cause more or less extensive injuries both on the surface and in depth. One of these lesions is gingival hypergrowth. Early injuries concern only the superficial periodontium and are represented by mild or moderate inflammation, gingival hypergrowth, which can be reversible after removing the irritating factor (bacterial plaque, tartar). Advanced injuries are characterized by major clinical, radiological and tissue changes that cause the destruction of the deep periodontium (alveolar bone, deep ligament). Hypergrowth changes may occur at the epithelial level with reduced conjunctival reaction or may predominantly involve fibro-connective structures of the chorion with insignificant reaction in the epithelial component. Through this study, we highlight superficial and deep changes at the gingival and periodontal level.

{"title":"Gingival overgrowth in fixed orthodontic therapy.","authors":"Alina Cristina Rădeanu, Ilona Mihaela Liliac, Maria Cristina Munteanu, Mihai Surpăţeanu, Ciprian Laurenţiu Pătru, Elena Cristina Andrei","doi":"10.47162/RJME.65.4.22","DOIUrl":"https://doi.org/10.47162/RJME.65.4.22","url":null,"abstract":"<p><p>The oral mucosa can suffer a series of traumatic injuries from various causes (bacterial plaque, tartar, fillings, incorrectly adapted prosthesis). A risk factor generating periodontal diseases is represented by fixed orthodontic therapy, if the forces exerted on it are excessive. These forces cause more or less extensive injuries both on the surface and in depth. One of these lesions is gingival hypergrowth. Early injuries concern only the superficial periodontium and are represented by mild or moderate inflammation, gingival hypergrowth, which can be reversible after removing the irritating factor (bacterial plaque, tartar). Advanced injuries are characterized by major clinical, radiological and tissue changes that cause the destruction of the deep periodontium (alveolar bone, deep ligament). Hypergrowth changes may occur at the epithelial level with reduced conjunctival reaction or may predominantly involve fibro-connective structures of the chorion with insignificant reaction in the epithelial component. Through this study, we highlight superficial and deep changes at the gingival and periodontal level.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"759-764"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434281","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sinonasal inverted papilloma from diagnosis to treatment - a narrative review.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.06
Mihail Tuşaliu, Carmen Aurelia Mogoantă, Camelia Iancu, Dan Iovănescu, Maria Niţescu, Cristian Bucur, Anca Cristina Perpelea, Ovidiu Lucian Cîmpeanu, Octavian Dragoş Palade

Inverted papilloma (IP) is a non-cancerous tumor that develops from the paranasal sinuses. Identifying and diagnosing an IP is vital for an ear, nose and throat specialist, due to its high recurrence rate and ability to transform into malignant carcinoma. Diagnosis is based on endonasal flexible endoscopy, preoperative biopsy, and imaging methods. Treatment is exclusively surgical, and its aim is the complete resection of the tumor to prevent further recurrences. The success of surgery depends on employing the most appropriate surgical technique. The choice should be tailored to the tumor's location, size, and the patient's specific anatomy. Endoscopic, open, or even combined approaches may be considered. Notably, attachment-oriented surgery is the cornerstone in endoscopic endonasal approaches. Regardless of the chosen approach, long-term surveillance is vital, as early detection provides the benefit of easier re-resection.

{"title":"Sinonasal inverted papilloma from diagnosis to treatment - a narrative review.","authors":"Mihail Tuşaliu, Carmen Aurelia Mogoantă, Camelia Iancu, Dan Iovănescu, Maria Niţescu, Cristian Bucur, Anca Cristina Perpelea, Ovidiu Lucian Cîmpeanu, Octavian Dragoş Palade","doi":"10.47162/RJME.65.4.06","DOIUrl":"https://doi.org/10.47162/RJME.65.4.06","url":null,"abstract":"<p><p>Inverted papilloma (IP) is a non-cancerous tumor that develops from the paranasal sinuses. Identifying and diagnosing an IP is vital for an ear, nose and throat specialist, due to its high recurrence rate and ability to transform into malignant carcinoma. Diagnosis is based on endonasal flexible endoscopy, preoperative biopsy, and imaging methods. Treatment is exclusively surgical, and its aim is the complete resection of the tumor to prevent further recurrences. The success of surgery depends on employing the most appropriate surgical technique. The choice should be tailored to the tumor's location, size, and the patient's specific anatomy. Endoscopic, open, or even combined approaches may be considered. Notably, attachment-oriented surgery is the cornerstone in endoscopic endonasal approaches. Regardless of the chosen approach, long-term surveillance is vital, as early detection provides the benefit of easier re-resection.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"599-607"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434367","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Late open conversion: a reliable solution for endoleak management after endovascular aortic aneurysm repair - a single center experience and literature review.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.11
Horaţiu Flaviu Coman, Octavian Aurel Andercou, Bogdan Stancu, Răzvan Alexandru Ciocan, Claudia Diana Gherman, Ana Trif, Moustafa Farran, Peter Lukas Haldenwang, Claudiu George Răşcanu

Background/objectives: Despite the efficacy of endovascular approaches for most secondary interventions post-endovascular aortic aneurysm repair (EVAR), a small proportion of patients need open conversion (OC) procedures. We shared our experience regarding patient outcomes after late OCs post-EVAR. We also performed a literature review of data published on this topic.

Patients, materials and methods: Medical records of patients who underwent late OCs post-EVAR at a Public Hospital in Germany (2017-2019) were retrospectively analyzed. OC involved total or partial endograft removal followed by aortic reconstruction. Preoperative patients' characteristics, indications for OC, and intra-∕post-operative outcomes were assessed. Studies published in English (2014-2024) on OCs post-EVAR complications were descriptively analyzed.

Results: Six patients underwent late OCs throughout the study (males: 66.67%; age [mean±standard deviation]: 66.50±2.89 years). Grafts were excised after a median of 72 months (range: 24-132 months), with 2∕6 (33.33%) urgent removals and 4∕6 (66.67%) elective. 4∕6 (66.67%) patients underwent complete removal, and 2∕6 (33.33%) were partial. Clamping site was suprarenal in 3∕6 (50.00%) patients, supraceliac in 2∕6 (33.33%), and infrarenal in 1∕6 (16.67%). Technical success was 100%, with 32 minutes mean clamping time and 1.67 L blood loss. Median follow-up was 13 months. No aneurysm growth was observed, and implanted grafts functioned well. 1∕6 (16.67%) patients died during the postoperative intensive care unit stay. Seven studies were included in our review. The 30-day mortality post-OCs was 6.2-10.0% in elective setting and up to 40% in urgent.

Conclusions: Late OC can be a reliable procedure for managing endoleak post-EVAR. Its success relies on accurate preoperative assessment and surgical expertise.

{"title":"Late open conversion: a reliable solution for endoleak management after endovascular aortic aneurysm repair - a single center experience and literature review.","authors":"Horaţiu Flaviu Coman, Octavian Aurel Andercou, Bogdan Stancu, Răzvan Alexandru Ciocan, Claudia Diana Gherman, Ana Trif, Moustafa Farran, Peter Lukas Haldenwang, Claudiu George Răşcanu","doi":"10.47162/RJME.65.4.11","DOIUrl":"https://doi.org/10.47162/RJME.65.4.11","url":null,"abstract":"<p><strong>Background/objectives: </strong>Despite the efficacy of endovascular approaches for most secondary interventions post-endovascular aortic aneurysm repair (EVAR), a small proportion of patients need open conversion (OC) procedures. We shared our experience regarding patient outcomes after late OCs post-EVAR. We also performed a literature review of data published on this topic.</p><p><strong>Patients, materials and methods: </strong>Medical records of patients who underwent late OCs post-EVAR at a Public Hospital in Germany (2017-2019) were retrospectively analyzed. OC involved total or partial endograft removal followed by aortic reconstruction. Preoperative patients' characteristics, indications for OC, and intra-∕post-operative outcomes were assessed. Studies published in English (2014-2024) on OCs post-EVAR complications were descriptively analyzed.</p><p><strong>Results: </strong>Six patients underwent late OCs throughout the study (males: 66.67%; age [mean±standard deviation]: 66.50±2.89 years). Grafts were excised after a median of 72 months (range: 24-132 months), with 2∕6 (33.33%) urgent removals and 4∕6 (66.67%) elective. 4∕6 (66.67%) patients underwent complete removal, and 2∕6 (33.33%) were partial. Clamping site was suprarenal in 3∕6 (50.00%) patients, supraceliac in 2∕6 (33.33%), and infrarenal in 1∕6 (16.67%). Technical success was 100%, with 32 minutes mean clamping time and 1.67 L blood loss. Median follow-up was 13 months. No aneurysm growth was observed, and implanted grafts functioned well. 1∕6 (16.67%) patients died during the postoperative intensive care unit stay. Seven studies were included in our review. The 30-day mortality post-OCs was 6.2-10.0% in elective setting and up to 40% in urgent.</p><p><strong>Conclusions: </strong>Late OC can be a reliable procedure for managing endoleak post-EVAR. Its success relies on accurate preoperative assessment and surgical expertise.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"647-654"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434355","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The impact of matrix metalloproteinases and their tissue inhibitors in patients with chronic glaucoma - a literature review.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.01
Teodor Cerbulescu, Andrei Anghel, Diduţa Alina Brie, Flavia Medana Petraşcu, Mădălina Casiana Salavat, Adina Iuliana Ardelean, Ileana Ramona Barac, Ovidiu Borugă

Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) play an important role in the pathophysiology of chronic glaucoma, as they are involved in extracellular matrix (ECM) remodeling in the trabecular meshwork (TM), affecting its ability to efficiently regulate intraocular pressure (IOP). Ensuring the balance between MMPs and TIMPs helps to maintain homeostasis in ocular tissues, which is essential to avoid glaucomatous lesions. Elevated levels of MMPs and increased degradation of the ECM, ultimately affecting aqueous humor outflow and increasing IOP, characterize glaucoma. In the current literature review, the impact and interactions of MMPs and TIMPs in chronic glaucoma have been emphasized, with multiple but still unelucidated roles in the mentioned pathology including their clinical implications, future research directions, and therapeutic approaches. Research to date indicates that the expression of TIMPs is altered in patients with chronic glaucoma, suggesting a compensatory response to increased MMPs activity. Certain drugs can influence the expression levels of MMPs and TIMPs, therefore therapeutic strategies can be developed to restore the balance between tissue enzymes and their inhibitors. Therefore, understanding the relationship between MMPs and TIMPs is a key factor in the pathogenesis of chronic glaucoma. Understanding the interplay between the two provides interesting insights into ECM remodeling in ocular tissues, highlighting the potential of targeted therapies to restore the balance between proteolytic enzymes and their inhibitors.

{"title":"The impact of matrix metalloproteinases and their tissue inhibitors in patients with chronic glaucoma - a literature review.","authors":"Teodor Cerbulescu, Andrei Anghel, Diduţa Alina Brie, Flavia Medana Petraşcu, Mădălina Casiana Salavat, Adina Iuliana Ardelean, Ileana Ramona Barac, Ovidiu Borugă","doi":"10.47162/RJME.65.4.01","DOIUrl":"https://doi.org/10.47162/RJME.65.4.01","url":null,"abstract":"<p><p>Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) play an important role in the pathophysiology of chronic glaucoma, as they are involved in extracellular matrix (ECM) remodeling in the trabecular meshwork (TM), affecting its ability to efficiently regulate intraocular pressure (IOP). Ensuring the balance between MMPs and TIMPs helps to maintain homeostasis in ocular tissues, which is essential to avoid glaucomatous lesions. Elevated levels of MMPs and increased degradation of the ECM, ultimately affecting aqueous humor outflow and increasing IOP, characterize glaucoma. In the current literature review, the impact and interactions of MMPs and TIMPs in chronic glaucoma have been emphasized, with multiple but still unelucidated roles in the mentioned pathology including their clinical implications, future research directions, and therapeutic approaches. Research to date indicates that the expression of TIMPs is altered in patients with chronic glaucoma, suggesting a compensatory response to increased MMPs activity. Certain drugs can influence the expression levels of MMPs and TIMPs, therefore therapeutic strategies can be developed to restore the balance between tissue enzymes and their inhibitors. Therefore, understanding the relationship between MMPs and TIMPs is a key factor in the pathogenesis of chronic glaucoma. Understanding the interplay between the two provides interesting insights into ECM remodeling in ocular tissues, highlighting the potential of targeted therapies to restore the balance between proteolytic enzymes and their inhibitors.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"557-565"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The intriguing perineurial cells - an updated overview of their origin, structure, functions and implication in pathology.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.02
Anne Marie Constantin, Adina Bianca Boşca, Carmen Bianca Crivii, Andreea Crintea, Rada Teodora Sufleţel, Bogdan Cătălin Alexandru, Alina Simona Şovrea

The paper overviews the uniquely intricate and distinct perineurium that envelops nerve fibers in bundles. It consists of perineurial cells (PCs), connective tissue, and blood vessels. The perineurium creates a microenvironment for efficient signal transmission, protects and maintains neuronal structure and function, and facilitates neuronal repair. PCs are a unique type of myofibroblasts essential for maintaining nerve homeostasis. They act as an effective blood-nerve barrier (BNB), protecting against toxins, infections, and mechanical trauma. Despite their crucial function, the origin, ultrastructure, molecular structure, and functional roles of PCs remain a mystery, making them a fascinating area of study.

{"title":"The intriguing perineurial cells - an updated overview of their origin, structure, functions and implication in pathology.","authors":"Anne Marie Constantin, Adina Bianca Boşca, Carmen Bianca Crivii, Andreea Crintea, Rada Teodora Sufleţel, Bogdan Cătălin Alexandru, Alina Simona Şovrea","doi":"10.47162/RJME.65.4.02","DOIUrl":"https://doi.org/10.47162/RJME.65.4.02","url":null,"abstract":"<p><p>The paper overviews the uniquely intricate and distinct perineurium that envelops nerve fibers in bundles. It consists of perineurial cells (PCs), connective tissue, and blood vessels. The perineurium creates a microenvironment for efficient signal transmission, protects and maintains neuronal structure and function, and facilitates neuronal repair. PCs are a unique type of myofibroblasts essential for maintaining nerve homeostasis. They act as an effective blood-nerve barrier (BNB), protecting against toxins, infections, and mechanical trauma. Despite their crucial function, the origin, ultrastructure, molecular structure, and functional roles of PCs remain a mystery, making them a fascinating area of study.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"567-574"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stroke as the first manifestation of an atrial myxoma. Review of the literature.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.04
Mihai Marius Botezat, Anca Maria Istrate-Ofiţeru, Larisa Iovan, Elena Cristina Andrei, Cristian Militaru, Emanuel Botezat, Marian Valentin Zorilă, Sebastian Militaru, Ilona Mihaela Liliac

Cardiac myxoma (CM) is the most common benign tumor of the heart and an important etiology of stroke in young adults. The study aimed to provide the latest literature data on CMs and, in particular, on the association between CM and cardioembolic ischemic stroke. It also discussed a specific instance of atrial myxoma (AM) in a young patient who suffered an ischemic stroke linked with familial cavernomatosis. The case presentation focuses on a 43-year-old woman showed up at the hospital's Emergency Room for transient speech disorders lasting about 15 minutes. The physical examination revealed preserved mental and cognitive status. Cranial magnetic resonance imaging (MRI) showed three areas of microvascular ischemia (frontal, parietal, and left occipital), in addition to multiple cavernomatous lesions. Because these microvascular ischemias were located in different vascular territories, we considered the cause to be embolic and completed the investigation with a transesophageal cardiac ultrasound that revealed a mobile and heterogeneous tumor mass in the left atrium. Histopathological investigation with immunohistochemistry proved the tumor to be a CM. The patient therapy included a multidisciplinary approach, which led to surgical excision of the tumor. The co-existence of cerebral cavernous malformations (CCMs) and AM might thus be coincidental or induced by a common genetic component. More cases are needed to verify or disprove the concept of a shared genetic basis for CCMs and myxoma.

{"title":"Stroke as the first manifestation of an atrial myxoma. Review of the literature.","authors":"Mihai Marius Botezat, Anca Maria Istrate-Ofiţeru, Larisa Iovan, Elena Cristina Andrei, Cristian Militaru, Emanuel Botezat, Marian Valentin Zorilă, Sebastian Militaru, Ilona Mihaela Liliac","doi":"10.47162/RJME.65.4.04","DOIUrl":"https://doi.org/10.47162/RJME.65.4.04","url":null,"abstract":"<p><p>Cardiac myxoma (CM) is the most common benign tumor of the heart and an important etiology of stroke in young adults. The study aimed to provide the latest literature data on CMs and, in particular, on the association between CM and cardioembolic ischemic stroke. It also discussed a specific instance of atrial myxoma (AM) in a young patient who suffered an ischemic stroke linked with familial cavernomatosis. The case presentation focuses on a 43-year-old woman showed up at the hospital's Emergency Room for transient speech disorders lasting about 15 minutes. The physical examination revealed preserved mental and cognitive status. Cranial magnetic resonance imaging (MRI) showed three areas of microvascular ischemia (frontal, parietal, and left occipital), in addition to multiple cavernomatous lesions. Because these microvascular ischemias were located in different vascular territories, we considered the cause to be embolic and completed the investigation with a transesophageal cardiac ultrasound that revealed a mobile and heterogeneous tumor mass in the left atrium. Histopathological investigation with immunohistochemistry proved the tumor to be a CM. The patient therapy included a multidisciplinary approach, which led to surgical excision of the tumor. The co-existence of cerebral cavernous malformations (CCMs) and AM might thus be coincidental or induced by a common genetic component. More cases are needed to verify or disprove the concept of a shared genetic basis for CCMs and myxoma.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"583-591"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434369","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biological and cytological-morphological assessment of tuberculous pleural effusions.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.17
Iancu Emil Pleşea, Elena Leocadia Pleşea, Răzvan Mihail Pleşea, Mircea Sebastian Şerbănescu, Marian Olaru, Dragoş Nicolosu, Gheorghe Gindrovel Dumitra, Valentin Titus Grigorean, Claudia Lucia Toma

Aim: Tuberculosis (TB) came back in the top of causes for infectious disease-related deaths and its pleural involvement is still in the top two extrapulmonary sites. The authors continued their studies on TB pleural effusions (Pl-Effs) with the assessment of biological and cytological variable of pleural fluid (PF), introducing in the investigation algorithm and testing a new tool, the computer-assisted evaluation of cell populations on PF smears.

Patients, materials and methods: A series of 85 patients with TB pleurisy (PLTB) were selected from a larger group of 322 patients with different types of Pl-Effs. The algorithm of investigation included. clinical variables, biological assays of PF, gross aspects including imagistic variables and PF cytology on May-Grünwald-Giemsa (MGG)-stained smears. All the data obtained were entered into and processed using Microsoft Excel module of the 2019 Microsoft Office Professional software along with the 2014 XLSTAT add-in program for MS Excel. The PF cellularity was assessed qualitatively by a cytologist and quantitatively with in-house software. Continuous variables were compared using Pearson's correlation test, while categorical variables were compared using χ² (chi-squared) test.

Results: Our analysis showed that patients were usually males, aged between 25 and 44 years with Pl-Eff discovered at clinical imagistic examination, almost always one-sided and free in the pleural cavity. Its extension was either moderate or reduced. The PF had a serous citrine appearance in most of the cases, and biological characteristics pleaded for an exudate [high levels of proteins and lactate dehydrogenase (LDH)], with elevated adenosine deaminase (ADA) values and rich in lymphocytes (Ly). The attempt to identify the pathogen in PF was not of much help. Apart from Ly, neutrophils [polymorphonuclear neutrophils (PMNs)] were a rare presence and their amount had only a trend of direct correlation with Ly. The same situation was encountered in the case of mesothelial cells (MCs). The comparison between the qualitative and the quantitative, computer-assisted evaluations of cytological smears showed that the results of the two methods overlapped in less than one third of the cases, although the sensitivity and specificity values as well as the two calculated predictive values of the qualitative method were encouraging.

Conclusions: The assessment of biological variables and cell populations of the PF are basic tools in the diagnosis of pleural TB. The assessment of PF cell population could be improved by the use of computer-assisted quantitative analysis of the PF smears, which is simple to design, easy to introduce and handle and reliable.

目的:肺结核(TB)再次成为传染病相关死亡的首要原因,其胸膜受累部位仍是肺外部位的前两名。作者继续对肺结核胸腔积液(Pl-Effs)进行研究,评估胸腔积液(PF)的生物学和细胞学变量,在调查算法中引入并测试一种新工具--计算机辅助评估胸腔积液涂片上的细胞群:从 322 名不同类型的肺结核胸膜炎患者中挑选了 85 名肺结核胸膜炎(PLTB)患者。调查算法包括:临床变量、PF 的生物检测、包括影像学变量在内的大体方面以及 May-Grünwald-Giemsa (MGG) 染色涂片上的 PF 细胞学。获得的所有数据均通过2019 Microsoft Office Professional软件的Microsoft Excel模块和2014 XLSTAT插件程序输入MS Excel并进行处理。PF细胞度由细胞学专家进行定性评估,并使用内部软件进行定量评估。连续变量的比较采用皮尔逊相关检验,分类变量的比较采用χ²(卡方)检验:我们的分析表明,患者通常为男性,年龄在 25 至 44 岁之间,在临床影像学检查中发现 Pl-Eff,几乎总是单侧且游离于胸膜腔内。其扩展程度为中等或缩小。大多数病例的胸膜积液呈浆液性黄水晶样,生物特征为渗出物[蛋白质和乳酸脱氢酶(LDH)含量高],腺苷脱氨酶(ADA)值升高,淋巴细胞(Ly)丰富。试图确定 PF 中的病原体并无多大帮助。除 Ly 外,中性粒细胞[多形核中性粒细胞(PMNs)]也很罕见,其数量与 Ly 仅有直接相关的趋势。间皮细胞(MCs)的情况也是如此。对细胞涂片进行定性和定量计算机辅助评估的比较结果显示,两种方法的结果重叠的病例不到三分之一,尽管定性方法的灵敏度和特异性值以及计算得出的两个预测值令人鼓舞:结论:对胸膜肺结核的生物变量和细胞群进行评估是诊断胸膜肺结核的基本工具。使用计算机辅助定量分析 PF 涂片可改进对 PF 细胞群的评估,这种方法设计简单、易于引入和操作,而且可靠。
{"title":"Biological and cytological-morphological assessment of tuberculous pleural effusions.","authors":"Iancu Emil Pleşea, Elena Leocadia Pleşea, Răzvan Mihail Pleşea, Mircea Sebastian Şerbănescu, Marian Olaru, Dragoş Nicolosu, Gheorghe Gindrovel Dumitra, Valentin Titus Grigorean, Claudia Lucia Toma","doi":"10.47162/RJME.65.4.17","DOIUrl":"https://doi.org/10.47162/RJME.65.4.17","url":null,"abstract":"<p><strong>Aim: </strong>Tuberculosis (TB) came back in the top of causes for infectious disease-related deaths and its pleural involvement is still in the top two extrapulmonary sites. The authors continued their studies on TB pleural effusions (Pl-Effs) with the assessment of biological and cytological variable of pleural fluid (PF), introducing in the investigation algorithm and testing a new tool, the computer-assisted evaluation of cell populations on PF smears.</p><p><strong>Patients, materials and methods: </strong>A series of 85 patients with TB pleurisy (PLTB) were selected from a larger group of 322 patients with different types of Pl-Effs. The algorithm of investigation included. clinical variables, biological assays of PF, gross aspects including imagistic variables and PF cytology on May-Grünwald-Giemsa (MGG)-stained smears. All the data obtained were entered into and processed using Microsoft Excel module of the 2019 Microsoft Office Professional software along with the 2014 XLSTAT add-in program for MS Excel. The PF cellularity was assessed qualitatively by a cytologist and quantitatively with in-house software. Continuous variables were compared using Pearson's correlation test, while categorical variables were compared using χ² (chi-squared) test.</p><p><strong>Results: </strong>Our analysis showed that patients were usually males, aged between 25 and 44 years with Pl-Eff discovered at clinical imagistic examination, almost always one-sided and free in the pleural cavity. Its extension was either moderate or reduced. The PF had a serous citrine appearance in most of the cases, and biological characteristics pleaded for an exudate [high levels of proteins and lactate dehydrogenase (LDH)], with elevated adenosine deaminase (ADA) values and rich in lymphocytes (Ly). The attempt to identify the pathogen in PF was not of much help. Apart from Ly, neutrophils [polymorphonuclear neutrophils (PMNs)] were a rare presence and their amount had only a trend of direct correlation with Ly. The same situation was encountered in the case of mesothelial cells (MCs). The comparison between the qualitative and the quantitative, computer-assisted evaluations of cytological smears showed that the results of the two methods overlapped in less than one third of the cases, although the sensitivity and specificity values as well as the two calculated predictive values of the qualitative method were encouraging.</p><p><strong>Conclusions: </strong>The assessment of biological variables and cell populations of the PF are basic tools in the diagnosis of pleural TB. The assessment of PF cell population could be improved by the use of computer-assisted quantitative analysis of the PF smears, which is simple to design, easy to introduce and handle and reliable.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"693-712"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Adenocarcinoma of the ileum: literature insights on pyloric gland metaplasia.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.05
Bogdan Stancu, Răzvan Alexandru Ciocan, Marius George Teodorescu, Doiniţa Crişan, Florin Vasile Mihăileanu, Ştefan Ursu, Liviu Tartacovschi, Ştefan Lucian Popa, Claudia Diana Gherman, Octavian Aurel Andercou

Adenocarcinoma (ADK) of the ileum is an infrequent cancer that poses significant diagnostic and treatment difficulties. This article analyses the existing case literature to investigate the correlation between pyloric gland metaplasia (PGM) and the onset of ileal ADK. PGM, defined by the atypical transformation of intestinal epithelial cells into gastric-type mucosa, has been recognized as a possible precursor lesion in the spectrum of several gastrointestinal malignancies. We intend to clarify the clinical characteristics, histological results, and outcomes linked to ileal ADK originating from PGM through an exhaustive examination of recorded cases. Our findings indicate that early identification of metaplastic alterations may be essential for enhancing prognosis and informing therapeutic choices. This study emphasizes the need for additional research to elucidate the mechanisms driving this transition and to improve diagnostic precision in clinical practice.

{"title":"Adenocarcinoma of the ileum: literature insights on pyloric gland metaplasia.","authors":"Bogdan Stancu, Răzvan Alexandru Ciocan, Marius George Teodorescu, Doiniţa Crişan, Florin Vasile Mihăileanu, Ştefan Ursu, Liviu Tartacovschi, Ştefan Lucian Popa, Claudia Diana Gherman, Octavian Aurel Andercou","doi":"10.47162/RJME.65.4.05","DOIUrl":"https://doi.org/10.47162/RJME.65.4.05","url":null,"abstract":"<p><p>Adenocarcinoma (ADK) of the ileum is an infrequent cancer that poses significant diagnostic and treatment difficulties. This article analyses the existing case literature to investigate the correlation between pyloric gland metaplasia (PGM) and the onset of ileal ADK. PGM, defined by the atypical transformation of intestinal epithelial cells into gastric-type mucosa, has been recognized as a possible precursor lesion in the spectrum of several gastrointestinal malignancies. We intend to clarify the clinical characteristics, histological results, and outcomes linked to ileal ADK originating from PGM through an exhaustive examination of recorded cases. Our findings indicate that early identification of metaplastic alterations may be essential for enhancing prognosis and informing therapeutic choices. This study emphasizes the need for additional research to elucidate the mechanisms driving this transition and to improve diagnostic precision in clinical practice.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"593-598"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434201","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electrophysiological parameters in patients with hepatic cirrhosis.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.16
Dragoş Lupu, Cristian Stănescu, Dănuţ Laurenţiu Nedelcu, George Alin Stoica, Mihai Marius Botezat, Andreea Ştefania Lupu

Various electrophysiological abnormalities are noted in patients with cirrhosis, the most prevalent consisting of QT prolongation and autonomic dysfunction. This study aims to thoroughly evaluate these abnormalities in cirrhotic patients by utilizing various parameters and compare them with healthy individuals. We evaluated 60 patients with hepatic cirrhosis using a resting electrocardiogram (ECG), ECG during and after the Valsalva maneuver, 24-hour ambulatory ECG monitoring and a standardized ECG stress test. We then compared these results with a group of 50 patients who had no hepatic cirrhosis or other significant known pathologies and were not on any medical treatment. At rest, cirrhotic patients had a reduced Valsalva index compared to the control group, but no statistical differences were noted in comparing resting heart rate (HR) values. At Holter monitoring, although there was a trend toward increased corrected QT (QTc) intervals in cirrhotic patients, it did not reach statistical significance, indicating no difference between the two groups. Reduced standard deviation of normal-to-normal (NN) intervals (SDNN) values, statistically significant, were noted in cirrhotic patients compared to the control group, indicating autonomic dysfunction. At stress test, there was no statistically significant difference in the results obtained for maximum HR during exercise between the two groups. Also, the results showed that cirrhotic patients had statistically significantly higher HR values after exercise compared to the control group. In conclusion, cirrhotic patients presented an increased grade of autonomic dysfunction compared to healthy patients, but no differences were noted regarding QT interval abnormalities.

{"title":"Electrophysiological parameters in patients with hepatic cirrhosis.","authors":"Dragoş Lupu, Cristian Stănescu, Dănuţ Laurenţiu Nedelcu, George Alin Stoica, Mihai Marius Botezat, Andreea Ştefania Lupu","doi":"10.47162/RJME.65.4.16","DOIUrl":"https://doi.org/10.47162/RJME.65.4.16","url":null,"abstract":"<p><p>Various electrophysiological abnormalities are noted in patients with cirrhosis, the most prevalent consisting of QT prolongation and autonomic dysfunction. This study aims to thoroughly evaluate these abnormalities in cirrhotic patients by utilizing various parameters and compare them with healthy individuals. We evaluated 60 patients with hepatic cirrhosis using a resting electrocardiogram (ECG), ECG during and after the Valsalva maneuver, 24-hour ambulatory ECG monitoring and a standardized ECG stress test. We then compared these results with a group of 50 patients who had no hepatic cirrhosis or other significant known pathologies and were not on any medical treatment. At rest, cirrhotic patients had a reduced Valsalva index compared to the control group, but no statistical differences were noted in comparing resting heart rate (HR) values. At Holter monitoring, although there was a trend toward increased corrected QT (QTc) intervals in cirrhotic patients, it did not reach statistical significance, indicating no difference between the two groups. Reduced standard deviation of normal-to-normal (NN) intervals (SDNN) values, statistically significant, were noted in cirrhotic patients compared to the control group, indicating autonomic dysfunction. At stress test, there was no statistically significant difference in the results obtained for maximum HR during exercise between the two groups. Also, the results showed that cirrhotic patients had statistically significantly higher HR values after exercise compared to the control group. In conclusion, cirrhotic patients presented an increased grade of autonomic dysfunction compared to healthy patients, but no differences were noted regarding QT interval abnormalities.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"687-692"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434264","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comprehensive insights into Pindborg tumor: etiology, advanced diagnostic approaches, and evidence-based management strategies - review of literature.
IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Pub Date : 2024-10-01 DOI: 10.47162/RJME.65.4.08
Cristian Niky Cumpătă, Maria Cristina Munteanu, Elena Cristina Andrei, Ilona Mihaela Liliac, Cristina Jana Busuioc, Paolo Di Francesco, Mădălina Anca Moldovan, Simona Iuliana Enache, Alexandru Burcea, Ciprian Laurenţiu Pătru, Călin Rareş Roman

Pindborg tumor is a calcifying epithelial odontogenic tumor possibly arising from developmental disturbances in dental lamina remnants. It predominantly affects individuals in their third decade of life, with women also experiencing later onset. The tumor exists in two forms, namely intraosseous (central) and extraosseous (peripheral), with the former showing higher post-surgery recurrence rates of about 14%. Despite its rarity, the tumor can be misdiagnosed due to symptoms resembling dental issues and headaches, or it may even be asymptomatic. Radiologically, it presents a mix of radiolucent and radiopaque areas, sometimes unilocular or multilocular. Histopathologically, it is characterized by nests and sheets of polygonal epithelial cells with eosinophilic cytoplasm and prominent nucleoli. The presence of eosinophilic amyloid-like material and calcifications is distinctive, ranging from small concretions to larger aggregates. The exact origin of amyloids is unknown, but they are thought to derive from degraded keratin filaments. Treatment varies by tumor location, with more invasive procedures required for jaw tumors, including bone resection, due to their aggressive growth and invasion of the surrounding tissues. Accurate, individualized treatment is crucial for patient outcomes, particularly in cases where the tumor's calcification is absent, indicating a severe impact on health. Our study included a case report of a 12-year-old patient who presented to the dental clinic complaining of sporadic pain in the area of the lower right front teeth. During a clinical examination of the area, we noticed a deformation of the alveolar bone, with a depressed mucosa. We followed the chronological steps of radiological examination, lesion excision, and histopathological examination to obtain a definitive diagnosis.

平堡瘤是一种钙化上皮性牙源性肿瘤,可能是由于牙齿薄层残留物的发育障碍引起的。这种肿瘤主要影响生命中第三个十年的人,女性发病较晚。该肿瘤有两种形式,即骨内(中央型)和骨外(周围型),前者的术后复发率较高,约为 14%。尽管这种肿瘤很罕见,但由于其症状类似牙科问题和头痛,甚至可能没有症状,因此可能会被误诊。在放射学上,它表现为放射线透明区和放射线不透明区的混合,有时为单眼或多眼。组织病理学上,它的特征是多角形上皮细胞的巢状和片状,胞质嗜酸性,核仁突出。嗜酸性淀粉样物质和钙化是该病的显著特征,从小凝块到较大的聚集体都有。淀粉样蛋白的确切来源尚不清楚,但认为它们来自降解的角蛋白丝。治疗方法因肿瘤位置而异,由于颌骨肿瘤具有侵袭性生长和对周围组织的侵袭,因此需要进行包括骨切除在内的侵入性手术。准确的个体化治疗对患者的预后至关重要,尤其是在肿瘤钙化缺失的情况下,预示着对健康的严重影响。我们的研究包括一例 12 岁患者的病例报告,该患者到牙科诊所就诊时主诉右下门牙部位零星疼痛。在对该区域进行临床检查时,我们发现牙槽骨变形,粘膜凹陷。我们按照放射学检查、病灶切除和组织病理学检查的时间顺序进行了检查,以获得明确诊断。
{"title":"Comprehensive insights into Pindborg tumor: etiology, advanced diagnostic approaches, and evidence-based management strategies - review of literature.","authors":"Cristian Niky Cumpătă, Maria Cristina Munteanu, Elena Cristina Andrei, Ilona Mihaela Liliac, Cristina Jana Busuioc, Paolo Di Francesco, Mădălina Anca Moldovan, Simona Iuliana Enache, Alexandru Burcea, Ciprian Laurenţiu Pătru, Călin Rareş Roman","doi":"10.47162/RJME.65.4.08","DOIUrl":"https://doi.org/10.47162/RJME.65.4.08","url":null,"abstract":"<p><p>Pindborg tumor is a calcifying epithelial odontogenic tumor possibly arising from developmental disturbances in dental lamina remnants. It predominantly affects individuals in their third decade of life, with women also experiencing later onset. The tumor exists in two forms, namely intraosseous (central) and extraosseous (peripheral), with the former showing higher post-surgery recurrence rates of about 14%. Despite its rarity, the tumor can be misdiagnosed due to symptoms resembling dental issues and headaches, or it may even be asymptomatic. Radiologically, it presents a mix of radiolucent and radiopaque areas, sometimes unilocular or multilocular. Histopathologically, it is characterized by nests and sheets of polygonal epithelial cells with eosinophilic cytoplasm and prominent nucleoli. The presence of eosinophilic amyloid-like material and calcifications is distinctive, ranging from small concretions to larger aggregates. The exact origin of amyloids is unknown, but they are thought to derive from degraded keratin filaments. Treatment varies by tumor location, with more invasive procedures required for jaw tumors, including bone resection, due to their aggressive growth and invasion of the surrounding tissues. Accurate, individualized treatment is crucial for patient outcomes, particularly in cases where the tumor's calcification is absent, indicating a severe impact on health. Our study included a case report of a 12-year-old patient who presented to the dental clinic complaining of sporadic pain in the area of the lower right front teeth. During a clinical examination of the area, we noticed a deformation of the alveolar bone, with a depressed mucosa. We followed the chronological steps of radiological examination, lesion excision, and histopathological examination to obtain a definitive diagnosis.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"617-625"},"PeriodicalIF":1.2,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143434229","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Romanian Journal of Morphology and Embryology
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