Cristina Annemari Popa, Nicoleta Ioana Andreescu, Teodora Smaranda Arghirescu, Carmen Angela Maria Petrescu, Cristian Marius Jincă, Emil Florin Huţ, Răzvan Gabriel Drăgoi, George Puenea, Daniel Popa
Acute lymphoblastic leukemia (ALL) is the most common type of leukemia in childhood and rare in adults, while acute myeloid leukemia (AML) is less common in children and more common in older adults. The aim of the study was to present our experience for the diagnostic of leukemia by using the classic and molecular cytogenetic methods. The study was conducted between 2009 and 2019 within the Classic and Molecular Genetic Laboratory of the Oncohematology Department from the Louis Ţurcanu Emergency Hospital for Children, Timişoara, Romania. The study group included 337 children and adults, evaluated between 2009 and 2019. By using the conventional and molecular cytogenetic technique, the cytogenetic anomalies found were 35 numerical chromosomal abnormalities, 10 (9;22)(q34;q11) [four ALL, one AML, five chronic myeloid leukemia (CML)] translocations, nine (15;17)(q24;q21) translocations, three (14;14)(q11;q32) translocations, two (4;11)(q21;q23) translocations, one (1;14)(p32;q11) translocation, one (7;14)(qter;q11) translocation, one (8;21)(q22;q22) translocation, one (9;14)(p12;q32) translocation, seven rearrangements of the MLL gene and two rearrangements of the core-binding factor subunit beta∕myosin heavy chain 11 (CBFB∕MYH11) gene. The use of conventional and molecular cytogenetic analysis is one of the most important prognostic indicators in acute leukemia patients, allowing the identification of biologically distinct subtypes of disease and selection of appropriate treatment approaches.
{"title":"Classic and molecular cytogenetic findings in leukemia patients from the Western part of Romania.","authors":"Cristina Annemari Popa, Nicoleta Ioana Andreescu, Teodora Smaranda Arghirescu, Carmen Angela Maria Petrescu, Cristian Marius Jincă, Emil Florin Huţ, Răzvan Gabriel Drăgoi, George Puenea, Daniel Popa","doi":"10.47162/RJME.65.2.06","DOIUrl":"10.47162/RJME.65.2.06","url":null,"abstract":"<p><p>Acute lymphoblastic leukemia (ALL) is the most common type of leukemia in childhood and rare in adults, while acute myeloid leukemia (AML) is less common in children and more common in older adults. The aim of the study was to present our experience for the diagnostic of leukemia by using the classic and molecular cytogenetic methods. The study was conducted between 2009 and 2019 within the Classic and Molecular Genetic Laboratory of the Oncohematology Department from the Louis Ţurcanu Emergency Hospital for Children, Timişoara, Romania. The study group included 337 children and adults, evaluated between 2009 and 2019. By using the conventional and molecular cytogenetic technique, the cytogenetic anomalies found were 35 numerical chromosomal abnormalities, 10 (9;22)(q34;q11) [four ALL, one AML, five chronic myeloid leukemia (CML)] translocations, nine (15;17)(q24;q21) translocations, three (14;14)(q11;q32) translocations, two (4;11)(q21;q23) translocations, one (1;14)(p32;q11) translocation, one (7;14)(qter;q11) translocation, one (8;21)(q22;q22) translocation, one (9;14)(p12;q32) translocation, seven rearrangements of the MLL gene and two rearrangements of the core-binding factor subunit beta∕myosin heavy chain 11 (CBFB∕MYH11) gene. The use of conventional and molecular cytogenetic analysis is one of the most important prognostic indicators in acute leukemia patients, allowing the identification of biologically distinct subtypes of disease and selection of appropriate treatment approaches.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"203-208"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384830/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Andrei Florin Părău, Amalia Raluca Ceauşu, Nela Puşa Gaje, Sorin Olariu, Marius Raica
Introduction: The varicose vein affects more than 30% of the general population. Significantly increased rates were noticed in women and older population. From the histopathological point of view, venous arterialization, smooth muscle cell hypertrophy, and hyperplasia are the main changes noticed in varicose vein disease. Some of the main therapeutic methods used in the management of varicose disease are injection sclerotherapy, conservative, surgical, saphenous vein inversion and removal, high saphenous ligation, ambulatory phlebectomy, transilluminated powered phlebectomy, endovascular management, cryostripping.
Aim: The aim of this study was to evaluate the morphology of connective fibers from the wall of the varicose veins extirpated by cryostripping.
Patients, materials and methods: The study included 109 samples taken by cryostripping method. Hematoxylin-Eosin, Masson's trichrome, Silver and Orcein staining were applied. The assessment of fibers was made according to score values between 0 and 3.
Results: It was found no major structural differences in terms of alterations of collagen fibers induced by the applied surgical procedure. It was noticed duplications and multiplications of the internal elastic lamina, as diffuse and nodular forms. Depletion of elastic fibers at the media was a lesion identified in most of the specimens. The depletion of reticulin fibers correlates with the accumulation of collagen fibers, which partially or completely replace the network in the media and intima. No correlation was found between changes in the reticulin network and the time between prelevation and buffered formalin fixation, the maximum time investigated being five days.
Conclusions: The Orcein staining in the venous vessel evaluation panel may be a useful investigation.
{"title":"The particularities of connective fibers from the wall of varicose veins extirpated by cryostripping.","authors":"Andrei Florin Părău, Amalia Raluca Ceauşu, Nela Puşa Gaje, Sorin Olariu, Marius Raica","doi":"10.47162/RJME.65.2.14","DOIUrl":"10.47162/RJME.65.2.14","url":null,"abstract":"<p><strong>Introduction: </strong>The varicose vein affects more than 30% of the general population. Significantly increased rates were noticed in women and older population. From the histopathological point of view, venous arterialization, smooth muscle cell hypertrophy, and hyperplasia are the main changes noticed in varicose vein disease. Some of the main therapeutic methods used in the management of varicose disease are injection sclerotherapy, conservative, surgical, saphenous vein inversion and removal, high saphenous ligation, ambulatory phlebectomy, transilluminated powered phlebectomy, endovascular management, cryostripping.</p><p><strong>Aim: </strong>The aim of this study was to evaluate the morphology of connective fibers from the wall of the varicose veins extirpated by cryostripping.</p><p><strong>Patients, materials and methods: </strong>The study included 109 samples taken by cryostripping method. Hematoxylin-Eosin, Masson's trichrome, Silver and Orcein staining were applied. The assessment of fibers was made according to score values between 0 and 3.</p><p><strong>Results: </strong>It was found no major structural differences in terms of alterations of collagen fibers induced by the applied surgical procedure. It was noticed duplications and multiplications of the internal elastic lamina, as diffuse and nodular forms. Depletion of elastic fibers at the media was a lesion identified in most of the specimens. The depletion of reticulin fibers correlates with the accumulation of collagen fibers, which partially or completely replace the network in the media and intima. No correlation was found between changes in the reticulin network and the time between prelevation and buffered formalin fixation, the maximum time investigated being five days.</p><p><strong>Conclusions: </strong>The Orcein staining in the venous vessel evaluation panel may be a useful investigation.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"273-278"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384038/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635826","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cristina Elena Negroiu, Robertina Iulia Tudoraşcu, Maria Cristina Beznă, Adrian Ionuţ Ungureanu, Sorina Octavia Honţaru, Suzana Dănoiu
Obesity poses a significant and escalating challenge in contemporary society, increasing the risk of developing various metabolic disorders such as dyslipidemia, cardiovascular diseases, non-alcoholic fatty liver disease (NAFLD), type 2 diabetes, and certain types of cancer. The current array of therapeutic interventions for obesity remains insufficient, prompting a pressing demand for novel and more effective treatments. In response, scientific attention has turned to the fibroblast growth factor 21 (FGF21) due to its remarkable and diverse impacts on lipid, carbohydrate, and energy metabolism. This comprehensive review aims to delve into the multifaceted aspects of FGF21, encompassing its discovery, synthesis, functional roles, and potential as a biomarker and therapeutic agent, with a specific focus on its implications for NAFLD.
{"title":"The role of FGF21 in the interplay between obesity and non-alcoholic fatty liver disease: a narrative review.","authors":"Cristina Elena Negroiu, Robertina Iulia Tudoraşcu, Maria Cristina Beznă, Adrian Ionuţ Ungureanu, Sorina Octavia Honţaru, Suzana Dănoiu","doi":"10.47162/RJME.65.2.02","DOIUrl":"10.47162/RJME.65.2.02","url":null,"abstract":"<p><p>Obesity poses a significant and escalating challenge in contemporary society, increasing the risk of developing various metabolic disorders such as dyslipidemia, cardiovascular diseases, non-alcoholic fatty liver disease (NAFLD), type 2 diabetes, and certain types of cancer. The current array of therapeutic interventions for obesity remains insufficient, prompting a pressing demand for novel and more effective treatments. In response, scientific attention has turned to the fibroblast growth factor 21 (FGF21) due to its remarkable and diverse impacts on lipid, carbohydrate, and energy metabolism. This comprehensive review aims to delve into the multifaceted aspects of FGF21, encompassing its discovery, synthesis, functional roles, and potential as a biomarker and therapeutic agent, with a specific focus on its implications for NAFLD.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"159-172"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384831/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635827","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alexandra Buruiană, Mircea Sebastian Şerbănescu, Bogdan Pop, Bogdan Alexandru Gheban, Carmen Georgiu, Doiniţa Crişan, Maria Crişan
Introduction: Histological grading of cutaneous squamous cell carcinoma (cSCC) is crucial for prognosis and treatment decisions, but manual grading is subjective and time-consuming.
Aim: This study aimed to develop and validate a deep learning (DL)-based model for automated cSCC grading, potentially improving diagnostic accuracy (ACC) and efficiency.
Materials and methods: Three deep neural networks (DNNs) with different architectures (AlexNet, GoogLeNet, ResNet-18) were trained using transfer learning on a dataset of 300 histopathological images of cSCC. The models were evaluated on their ACC, sensitivity (SN), specificity (SP), and area under the curve (AUC). Clinical validation was performed on 60 images, comparing the DNNs' predictions with those of a panel of pathologists.
Results: The models achieved high performance metrics (ACC>85%, SN>85%, SP>92%, AUC>97%) demonstrating their potential for objective and efficient cSCC grading. The high agreement between the DNNs and pathologists, as well as among different network architectures, further supports the reliability and ACC of the DL models. The top-performing models are publicly available, facilitating further research and potential clinical implementation.
Conclusions: This study highlights the promising role of DL in enhancing cSCC diagnosis, ultimately improving patient care.
{"title":"Automated cutaneous squamous cell carcinoma grading using deep learning with transfer learning.","authors":"Alexandra Buruiană, Mircea Sebastian Şerbănescu, Bogdan Pop, Bogdan Alexandru Gheban, Carmen Georgiu, Doiniţa Crişan, Maria Crişan","doi":"10.47162/RJME.65.2.10","DOIUrl":"10.47162/RJME.65.2.10","url":null,"abstract":"<p><strong>Introduction: </strong>Histological grading of cutaneous squamous cell carcinoma (cSCC) is crucial for prognosis and treatment decisions, but manual grading is subjective and time-consuming.</p><p><strong>Aim: </strong>This study aimed to develop and validate a deep learning (DL)-based model for automated cSCC grading, potentially improving diagnostic accuracy (ACC) and efficiency.</p><p><strong>Materials and methods: </strong>Three deep neural networks (DNNs) with different architectures (AlexNet, GoogLeNet, ResNet-18) were trained using transfer learning on a dataset of 300 histopathological images of cSCC. The models were evaluated on their ACC, sensitivity (SN), specificity (SP), and area under the curve (AUC). Clinical validation was performed on 60 images, comparing the DNNs' predictions with those of a panel of pathologists.</p><p><strong>Results: </strong>The models achieved high performance metrics (ACC>85%, SN>85%, SP>92%, AUC>97%) demonstrating their potential for objective and efficient cSCC grading. The high agreement between the DNNs and pathologists, as well as among different network architectures, further supports the reliability and ACC of the DL models. The top-performing models are publicly available, facilitating further research and potential clinical implementation.</p><p><strong>Conclusions: </strong>This study highlights the promising role of DL in enhancing cSCC diagnosis, ultimately improving patient care.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"243-250"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384044/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635789","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Paul Alexandru Deme, Dan Ioan Fruja, Nicolae Cătălin Hreniuc, Graţian Cosmin Damian, Florin Mihai Marcu, Roland Fazakas, Casiana Boru, Nicoleta Zurbău-Anghel, Alexandru Mircea Pop
In this comprehensive case report, we examine a 29-year-old male who suffered a high-energy vehicular accident, resulting in a type III Hawkins fracture of the talus. This specific fracture type is critically associated with a greater than 90% risk of progressing to avascular necrosis (AVN) of the talus, a severe and debilitating condition. Alongside this, the patient sustained fractures of the medial and lateral malleolus. Due to extensive swelling and severe circulatory disorders, an immediate emergency surgical procedure was necessitated, employing nail fixation as a stabilizing intervention. Over the course of 12 months following the surgery, despite routine post-operative imaging including X-rays and computed tomography (CT) scans, the patient continued to experience significant pain and impairment. This condition led to further investigations, culminating in a magnetic resonance imaging (MRI) that revealed an area of 19.8∕20.9 mm of AVN on the talus dome's upper-lateral facet. Interestingly, earlier CT scans had indicated multiple osteitic lesions, but these findings lacked a clear clinical correspondence, presenting a diagnostic challenge. To resolve this ambiguity and to definitively distinguish between necrosis and infection, a targeted histopathological analysis was deemed necessary. This analysis was conducted on a bone fragment extracted during a follow-up surgical procedure for nail removal. The results from this analysis present an area of bone and myeloid tissue necrosis unequivocally confirming the presence of AVN, effectively ruling out osteitis as a potential diagnosis. This critical diagnostic clarification allowed for a shift in therapeutic strategy, enabling the initiation of a more focused and potentially curative treatment regimen.
在这份综合病例报告中,我们对一名 29 岁的男性进行了研究,他遭遇了一起高能量车祸,导致距骨 III 型霍金斯骨折。这种特殊的骨折类型与 90% 以上的距骨血管性坏死(AVN)风险密切相关,AVN 是一种严重的致残性疾病。与此同时,患者的内侧和外侧踝骨也发生了骨折。由于大面积肿胀和严重的循环障碍,必须立即进行紧急手术,采用钉子固定作为稳定干预措施。在手术后的 12 个月里,尽管进行了常规的术后影像学检查,包括 X 光和计算机断层扫描(CT),但患者仍然感到明显的疼痛和功能障碍。这种情况导致了进一步的检查,最终在磁共振成像(MRI)中发现距骨穹隆上外侧面有一个面积为 19.8∕20.9 mm 的 AVN。有趣的是,早前的 CT 扫描显示有多处骨质病变,但这些结果缺乏明确的临床对应关系,给诊断带来了挑战。为了解决这一模糊问题并明确区分坏死和感染,有必要进行有针对性的组织病理学分析。这项分析是在拔钉的后续手术过程中提取的一块骨片上进行的。分析结果显示,骨和髓质组织坏死区域明确证实了 AVN 的存在,有效排除了骨炎的潜在诊断。这一重要的诊断结果有助于改变治疗策略,使治疗方案更有针对性,并有可能达到治愈效果。
{"title":"Post-traumatic avascular necrosis of the talus.","authors":"Paul Alexandru Deme, Dan Ioan Fruja, Nicolae Cătălin Hreniuc, Graţian Cosmin Damian, Florin Mihai Marcu, Roland Fazakas, Casiana Boru, Nicoleta Zurbău-Anghel, Alexandru Mircea Pop","doi":"10.47162/RJME.65.2.23","DOIUrl":"10.47162/RJME.65.2.23","url":null,"abstract":"<p><p>In this comprehensive case report, we examine a 29-year-old male who suffered a high-energy vehicular accident, resulting in a type III Hawkins fracture of the talus. This specific fracture type is critically associated with a greater than 90% risk of progressing to avascular necrosis (AVN) of the talus, a severe and debilitating condition. Alongside this, the patient sustained fractures of the medial and lateral malleolus. Due to extensive swelling and severe circulatory disorders, an immediate emergency surgical procedure was necessitated, employing nail fixation as a stabilizing intervention. Over the course of 12 months following the surgery, despite routine post-operative imaging including X-rays and computed tomography (CT) scans, the patient continued to experience significant pain and impairment. This condition led to further investigations, culminating in a magnetic resonance imaging (MRI) that revealed an area of 19.8∕20.9 mm of AVN on the talus dome's upper-lateral facet. Interestingly, earlier CT scans had indicated multiple osteitic lesions, but these findings lacked a clear clinical correspondence, presenting a diagnostic challenge. To resolve this ambiguity and to definitively distinguish between necrosis and infection, a targeted histopathological analysis was deemed necessary. This analysis was conducted on a bone fragment extracted during a follow-up surgical procedure for nail removal. The results from this analysis present an area of bone and myeloid tissue necrosis unequivocally confirming the presence of AVN, effectively ruling out osteitis as a potential diagnosis. This critical diagnostic clarification allowed for a shift in therapeutic strategy, enabling the initiation of a more focused and potentially curative treatment regimen.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"349-352"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384039/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635820","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Iulian Prutianu, Simona Eliza Giuşcă, Bogdan Gafton, Mariana Bianca Chifu, Cristina Terinte, Alexandra Antonescu, Larisa Popovici, Irina Draga Căruntu
Triple-negative breast cancer (BC) represents an extensively analyzed entity to establish the overall framework of clinicopathological characteristics, with an impact on defining prognostic and predictive factors. The relationship between triple-negative BC and androgen receptor (AR) is far from being clarified. We aimed to evaluate the classical clinicopathological spectrum that characterized a triple-negative BC, focusing on AR expression. The study group comprised 124 cases of triple-negative BC. The main clinicopathological parameters were extracted from medical records. The immunohistochemical (IHC) exam was run using the following antibodies: anti-estrogen receptor (ER), anti-progesterone receptor (PR), anti-human epidermal growth factor receptor (HER2∕neu), anti-Ki67 and anti-AR. AR immunoexpression was assessed as absent (completely negative) or present (unrelated to percentages and intensity). Data were statistically analyzed. AR expression was positive in 78 (63%) cases and negative in 46 (37%) cases. Among the study group, 28 cases exhibited an AR percentage ranging from 1% to 10%, 15 cases showed a percentage between 11% and 50%, while 12 cases had AR values between 51% and 75% and 23 cases fell within the AR range of 76% to 100%. No significant differences between AR immunoexpression (negative versus positive), clinicopathological characteristics and survival parameters were found. Statistically significant differences were registered between histological type, tumor stage, distant metastasis, tumor-infiltrating lymphocytes (TILs), treatment and residual cancer burden (RCB), and survival parameters. Thus, our results sustain that AR does not affect the biological behavior of triple-negative BC.
三阴性乳腺癌(BC)是一个被广泛分析的实体,其临床病理特征的整体框架对确定预后和预测因素具有重要影响。三阴性乳腺癌与雄激素受体(AR)之间的关系远未明确。我们的目的是评估三阴性 BC 的经典临床病理特征,重点关注 AR 的表达。研究组包括124例三阴性BC。主要临床病理参数来自病历。使用以下抗体进行免疫组化(IHC)检查:抗雌激素受体(ER)、抗孕酮受体(PR)、抗人表皮生长因子受体(HER2∕neu)、抗Ki67和抗AR。AR免疫表达被评估为不存在(完全阴性)或存在(与百分比和强度无关)。对数据进行了统计分析。78例(63%)AR表达阳性,46例(37%)阴性。在研究组中,28 个病例的 AR 百分比在 1%-10%之间,15 个病例的 AR 百分比在 11%-50%之间,12 个病例的 AR 值在 51%-75%之间,23 个病例的 AR 值在 76%-100%之间。AR免疫表达(阴性与阳性)、临床病理特征和生存参数之间没有发现明显差异。组织学类型、肿瘤分期、远处转移、肿瘤浸润淋巴细胞(TILs)、治疗和残余癌负荷(RCB)与生存参数之间存在统计学意义上的差异。因此,我们的研究结果表明,AR 不会影响三阴性 BC 的生物学行为。
{"title":"Triple-negative breast cancer: from classical clinicopathological features to androgen receptor profile.","authors":"Iulian Prutianu, Simona Eliza Giuşcă, Bogdan Gafton, Mariana Bianca Chifu, Cristina Terinte, Alexandra Antonescu, Larisa Popovici, Irina Draga Căruntu","doi":"10.47162/RJME.65.2.07","DOIUrl":"10.47162/RJME.65.2.07","url":null,"abstract":"<p><p>Triple-negative breast cancer (BC) represents an extensively analyzed entity to establish the overall framework of clinicopathological characteristics, with an impact on defining prognostic and predictive factors. The relationship between triple-negative BC and androgen receptor (AR) is far from being clarified. We aimed to evaluate the classical clinicopathological spectrum that characterized a triple-negative BC, focusing on AR expression. The study group comprised 124 cases of triple-negative BC. The main clinicopathological parameters were extracted from medical records. The immunohistochemical (IHC) exam was run using the following antibodies: anti-estrogen receptor (ER), anti-progesterone receptor (PR), anti-human epidermal growth factor receptor (HER2∕neu), anti-Ki67 and anti-AR. AR immunoexpression was assessed as absent (completely negative) or present (unrelated to percentages and intensity). Data were statistically analyzed. AR expression was positive in 78 (63%) cases and negative in 46 (37%) cases. Among the study group, 28 cases exhibited an AR percentage ranging from 1% to 10%, 15 cases showed a percentage between 11% and 50%, while 12 cases had AR values between 51% and 75% and 23 cases fell within the AR range of 76% to 100%. No significant differences between AR immunoexpression (negative versus positive), clinicopathological characteristics and survival parameters were found. Statistically significant differences were registered between histological type, tumor stage, distant metastasis, tumor-infiltrating lymphocytes (TILs), treatment and residual cancer burden (RCB), and survival parameters. Thus, our results sustain that AR does not affect the biological behavior of triple-negative BC.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"209-216"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384857/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635878","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aifer Cherim, Alexandra Eugenia Bastian, Cristiana Gabriela Popp, Maia Ioana Mihon, Ion Cristian Efrem, Ananu Florentin Vreju, Răzvan Adrian Ionescu
Eosinophilic fasciitis (EF) remains a diagnostic challenge due to its rarity and resemblance to scleroderma. This case report aims to provide a cohesive exploration of EF's clinical nuances, emphasizing the importance of accurate diagnosis and effective management. A 52-year-old male developed bilateral forearm and calf hardening, along with erythema, pruritus, and pain four months prior to the presentation in our Clinic. The symptoms initially debuted bilaterally in the forearms and progressed to involve the calves, distal arms, and thighs. Clinical examination revealed symmetrical plaques on forearms and calves, featuring erythematous, hyper, and hypopigmented elements extending proximally, a positive "groove sign" and a moderate difficulty in knee joint flexion. Despite these findings, the patient was generally in good condition, without any other notable clinical signs. Initial laboratory findings showed slightly increased percentual eosinophil levels, elevated C-reactive protein (CRP), normal erythrocyte sedimentation rate (ESR), and negative antinuclear and scleroderma specific antibodies. Magnetic resonance imaging (MRI) demonstrated enhanced fascial signal and thickening while the fascia-muscle biopsy revealed marked edema and inflammatory lymphoplasmacytic infiltrate, consistent with the diagnosis of EF. The patient showed a favorable response to systemic corticosteroids. EF predominantly affects males aged 30 to 60 and is characterized by a sudden onset and unclear etiological factors. Differential diagnosis requires careful exclusion of scleroderma and other mimicking conditions. Diagnostic modalities such as skin-muscle biopsy and MRI reveal characteristic findings like inflammatory infiltrate and fascial thickening. Accurate diagnosis and differentiation from scleroderma are crucial, with early intervention involving glucocorticoids and immunosuppressive agents improving long-term outcomes.
嗜酸性粒细胞筋膜炎(EF)因其罕见性和与硬皮病的相似性,仍然是诊断上的一个难题。本病例报告旨在深入探讨嗜酸性粒细胞性筋膜炎的临床细微差别,强调准确诊断和有效治疗的重要性。一名 52 岁的男性在本诊所就诊前四个月出现双侧前臂和小腿变硬,并伴有红斑、瘙痒和疼痛。症状最初出现在双侧前臂,后来发展到小腿、手臂远端和大腿。临床检查发现,前臂和小腿出现对称性斑块,红斑、色素沉着和色素减退,向近端延伸,"凹槽征 "阳性,膝关节屈曲中度困难。尽管有这些发现,但患者总体状况良好,没有其他明显的临床症状。初步实验室检查结果显示,嗜酸性粒细胞水平略有升高,C反应蛋白(CRP)升高,红细胞沉降率(ESR)正常,抗核抗体和硬皮病特异性抗体阴性。磁共振成像(MRI)显示筋膜信号增强且增厚,筋膜肌肉活检显示明显水肿和炎性淋巴浆细胞浸润,与 EF 诊断一致。患者对全身皮质类固醇的反应良好。EF主要影响30至60岁的男性,其特点是发病突然,病因不明。鉴别诊断需要仔细排除硬皮病和其他类似疾病。皮肤肌肉活检和核磁共振成像等诊断方法可发现炎症浸润和筋膜增厚等特征性结果。准确诊断和与硬皮病的鉴别至关重要,使用糖皮质激素和免疫抑制剂进行早期干预可改善长期预后。
{"title":"Eosinophilic fasciitis: unraveling the clinical tapestry of a rare case and review of literature.","authors":"Aifer Cherim, Alexandra Eugenia Bastian, Cristiana Gabriela Popp, Maia Ioana Mihon, Ion Cristian Efrem, Ananu Florentin Vreju, Răzvan Adrian Ionescu","doi":"10.47162/RJME.65.2.22","DOIUrl":"10.47162/RJME.65.2.22","url":null,"abstract":"<p><p>Eosinophilic fasciitis (EF) remains a diagnostic challenge due to its rarity and resemblance to scleroderma. This case report aims to provide a cohesive exploration of EF's clinical nuances, emphasizing the importance of accurate diagnosis and effective management. A 52-year-old male developed bilateral forearm and calf hardening, along with erythema, pruritus, and pain four months prior to the presentation in our Clinic. The symptoms initially debuted bilaterally in the forearms and progressed to involve the calves, distal arms, and thighs. Clinical examination revealed symmetrical plaques on forearms and calves, featuring erythematous, hyper, and hypopigmented elements extending proximally, a positive \"groove sign\" and a moderate difficulty in knee joint flexion. Despite these findings, the patient was generally in good condition, without any other notable clinical signs. Initial laboratory findings showed slightly increased percentual eosinophil levels, elevated C-reactive protein (CRP), normal erythrocyte sedimentation rate (ESR), and negative antinuclear and scleroderma specific antibodies. Magnetic resonance imaging (MRI) demonstrated enhanced fascial signal and thickening while the fascia-muscle biopsy revealed marked edema and inflammatory lymphoplasmacytic infiltrate, consistent with the diagnosis of EF. The patient showed a favorable response to systemic corticosteroids. EF predominantly affects males aged 30 to 60 and is characterized by a sudden onset and unclear etiological factors. Differential diagnosis requires careful exclusion of scleroderma and other mimicking conditions. Diagnostic modalities such as skin-muscle biopsy and MRI reveal characteristic findings like inflammatory infiltrate and fascial thickening. Accurate diagnosis and differentiation from scleroderma are crucial, with early intervention involving glucocorticoids and immunosuppressive agents improving long-term outcomes.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"341-347"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384037/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635791","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Adina Elena Tănase, Iustina Petra Solomon-Condriuc, Raluca Anamaria Mogoş, Gabriel Costăchescu, Cristina David, Cătălin Mihai Buzdugă, Dragoş Viorel Scripcariu, Claudia Florida Costea, Andrei Ionuţ Cucu, Gabriel Valentin Tănase, Daniela Maria Tănase, Dragoş Nemescu, Ana Maria Dumitrescu, Alexandru Cărăuleanu
Introduction: Literature data present new studies about precancerous lesions of pelvic serous carcinoma that originate from the tubal secretory cells. It has long been thought that ovarian cancer cannot be prevented by prophylactic screening or surgery. In recent years, gynecologists have adapted to new principles and so, during routine hysterectomies in perimenopausal women for benign uterine pathologies, salpingo-oophorectomy is performed as a prophylactic approach.
Aim: The purpose of our article was to draw attention to the association between abnormal fallopian tube pathology and the presence of serous ovarian neoplasia in perimenopausal women at risk.
Case presentation: We report the case of a 45-year-old woman who had unspecific symptoms of abdominal pain and loss of appetite and weight. A pelvic magnetic resonance imaging was performed, and an ovarian mass was detected. Our case shows that the fallopian tube can be the primary point of origin for a pelvic disease, therefore prevention is possible with early computed tomography scan and annual ultrasound. The patient presented with a T1c staging post-surgery and her chances of survival could have decreased if she had postponed medical examination longer. We found a significant increase in the absolute number of tubal secretory cells in patients with ovarian neoplasia, which supports the assumption that serous tubal intraepithelial carcinoma lesions are found especially in the serous ovarian type.
Conclusions: Our article is a strong suggestion that serous ovarian cancer originates from the fallopian tube and can potentially serve as a sensitive biomarker for early serous carcinogenesis within the fallopian tube.
{"title":"High-grade serous ovarian cancer (HGSOC) with fallopian tube involvement.","authors":"Adina Elena Tănase, Iustina Petra Solomon-Condriuc, Raluca Anamaria Mogoş, Gabriel Costăchescu, Cristina David, Cătălin Mihai Buzdugă, Dragoş Viorel Scripcariu, Claudia Florida Costea, Andrei Ionuţ Cucu, Gabriel Valentin Tănase, Daniela Maria Tănase, Dragoş Nemescu, Ana Maria Dumitrescu, Alexandru Cărăuleanu","doi":"10.47162/RJME.65.2.20","DOIUrl":"10.47162/RJME.65.2.20","url":null,"abstract":"<p><strong>Introduction: </strong>Literature data present new studies about precancerous lesions of pelvic serous carcinoma that originate from the tubal secretory cells. It has long been thought that ovarian cancer cannot be prevented by prophylactic screening or surgery. In recent years, gynecologists have adapted to new principles and so, during routine hysterectomies in perimenopausal women for benign uterine pathologies, salpingo-oophorectomy is performed as a prophylactic approach.</p><p><strong>Aim: </strong>The purpose of our article was to draw attention to the association between abnormal fallopian tube pathology and the presence of serous ovarian neoplasia in perimenopausal women at risk.</p><p><strong>Case presentation: </strong>We report the case of a 45-year-old woman who had unspecific symptoms of abdominal pain and loss of appetite and weight. A pelvic magnetic resonance imaging was performed, and an ovarian mass was detected. Our case shows that the fallopian tube can be the primary point of origin for a pelvic disease, therefore prevention is possible with early computed tomography scan and annual ultrasound. The patient presented with a T1c staging post-surgery and her chances of survival could have decreased if she had postponed medical examination longer. We found a significant increase in the absolute number of tubal secretory cells in patients with ovarian neoplasia, which supports the assumption that serous tubal intraepithelial carcinoma lesions are found especially in the serous ovarian type.</p><p><strong>Conclusions: </strong>Our article is a strong suggestion that serous ovarian cancer originates from the fallopian tube and can potentially serve as a sensitive biomarker for early serous carcinogenesis within the fallopian tube.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"325-329"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384032/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635794","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
George Alexandru Croitoru, Diana Cristina Pîrvulescu, Adelina Gabriela Niculescu, Alexandru Mihai Grumezescu, Alexandru Mihai Antohi, Carmen Larisa Nicolae
This paper explores the integral role of metallic nanomaterials in drug delivery, specifically focusing on their unique characteristics and applications. Exhibiting unique size, shape, and surface features, metallic nanoparticles (MNPs) (e.g., gold, iron oxide, and silver NPs) present possibilities for improving medication efficacy while minimizing side effects. Their demonstrated success in improving drug solubility, bioavailability, and targeted release makes them promising carriers for treating a variety of diseases, including inflammation and cancer, which has one of the highest rates of mortality in the world. Furthermore, it is crucial to acknowledge some limitations of MNPs in drug delivery before successfully incorporating them into standard medical procedures. Thus, challenges such as potential toxicity, issues related to long-term safety, and the need for standardized production methods will also be addressed.
{"title":"Metallic nanomaterials - targeted drug delivery approaches for improved bioavailability, reduced side toxicity, and enhanced patient outcomes.","authors":"George Alexandru Croitoru, Diana Cristina Pîrvulescu, Adelina Gabriela Niculescu, Alexandru Mihai Grumezescu, Alexandru Mihai Antohi, Carmen Larisa Nicolae","doi":"10.47162/RJME.65.2.01","DOIUrl":"10.47162/RJME.65.2.01","url":null,"abstract":"<p><p>This paper explores the integral role of metallic nanomaterials in drug delivery, specifically focusing on their unique characteristics and applications. Exhibiting unique size, shape, and surface features, metallic nanoparticles (MNPs) (e.g., gold, iron oxide, and silver NPs) present possibilities for improving medication efficacy while minimizing side effects. Their demonstrated success in improving drug solubility, bioavailability, and targeted release makes them promising carriers for treating a variety of diseases, including inflammation and cancer, which has one of the highest rates of mortality in the world. Furthermore, it is crucial to acknowledge some limitations of MNPs in drug delivery before successfully incorporating them into standard medical procedures. Thus, challenges such as potential toxicity, issues related to long-term safety, and the need for standardized production methods will also be addressed.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"145-158"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384046/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635796","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Diduţa Alina Brie, Adelina Maria Jianu, Roxana Popescu, Teodor Cerbulescu, Sorin Dema, Daniel Miron Brie, Veronica Mădălina Borugă
An aneurysm is defined as a dilation of the arterial wall with a diameter exceeding 1.5 times the normal diameter of the vessel concerned. Aortic aneurysms (AAs) can develop at any level but are mostly found at the abdominal and infrarenal levels and extend to the iliac arteries. AAs are usually asymptomatic and are most often discovered incidentally during various imaging investigations for other conditions. Rupture of an AA is usually dramatic, being one of the causes of sudden cardiac death. Surgical treatment and, more recently, endovascular treatment are the only effective methods of AA repair. In this study, we screened for the diagnosis of AAs in patients with stable exertional angina who had indications for coronary angiography. The study was carried out in the period 2021-2023 in the Institute of Cardiovascular Diseases Timişoara, Romania. Of the 2458 patients with exertional angina who required coronary angiography, a number of 1844 (75%) patients had at least one stenotic atheromatous plaque, and of these 312 patients had AAs, of which 173 at the level of the abdominal aorta.
动脉瘤的定义是动脉壁扩张,直径超过相关血管正常直径的 1.5 倍。主动脉瘤(AA)可发生在任何部位,但大多位于腹部和肾下部,并延伸至髂动脉。主动脉瘤通常没有症状,最常见的情况是在对其他疾病进行各种成像检查时偶然发现。AA 的破裂通常很剧烈,是导致心脏性猝死的原因之一。手术治疗以及最近的血管内治疗是修复 AA 的唯一有效方法。在这项研究中,我们对有冠状动脉造影指征的稳定型劳累性心绞痛患者进行了 AA 诊断筛查。研究于 2021-2023 年期间在罗马尼亚蒂米什瓦拉心血管疾病研究所进行。在需要进行冠状动脉造影的 2458 名劳累性心绞痛患者中,有 1844 名患者(75%)至少有一个动脉粥样斑块狭窄,其中 312 名患者有 AA,其中 173 名患者位于腹主动脉水平。
{"title":"Aortic aneurysms in patients with atherosclerotic coronary artery disease in the southwestern region of Romania - clinical and histopathological study.","authors":"Diduţa Alina Brie, Adelina Maria Jianu, Roxana Popescu, Teodor Cerbulescu, Sorin Dema, Daniel Miron Brie, Veronica Mădălina Borugă","doi":"10.47162/RJME.65.2.11","DOIUrl":"10.47162/RJME.65.2.11","url":null,"abstract":"<p><p>An aneurysm is defined as a dilation of the arterial wall with a diameter exceeding 1.5 times the normal diameter of the vessel concerned. Aortic aneurysms (AAs) can develop at any level but are mostly found at the abdominal and infrarenal levels and extend to the iliac arteries. AAs are usually asymptomatic and are most often discovered incidentally during various imaging investigations for other conditions. Rupture of an AA is usually dramatic, being one of the causes of sudden cardiac death. Surgical treatment and, more recently, endovascular treatment are the only effective methods of AA repair. In this study, we screened for the diagnosis of AAs in patients with stable exertional angina who had indications for coronary angiography. The study was carried out in the period 2021-2023 in the Institute of Cardiovascular Diseases Timişoara, Romania. Of the 2458 patients with exertional angina who required coronary angiography, a number of 1844 (75%) patients had at least one stenotic atheromatous plaque, and of these 312 patients had AAs, of which 173 at the level of the abdominal aorta.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 2","pages":"251-256"},"PeriodicalIF":1.2,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384034/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635788","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}