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Histopathology of Hidradenitis Suppurativa: A Systematic Review. 化脓性汗腺炎的组织病理学:系统综述。
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-07-14 DOI: 10.3390/dermatopathology9030029
Shane David Basil Smith, Ginette A Okoye, Olayemi Sokumbi

Hidradenitis suppurativa (HS) is a chronic inflammatory scarring disease felt to be related to occlusion of the hair follicle unit in intertriginous areas. We perform a systematic review on HS histopathology to evaluate current knowledge and discuss future directions. PubMed and Scopus databases were searched for relevant articles published from January 1985 to January 2021 that discussed the pathology of HS. Additional articles were identified by hand-searching, which entailed manually scanning selected journals. A total of 355 citations were identified in the primary search within the main databases. Two hundred and seventy-nine articles were excluded after a review of titles, abstracts, and duplicates. Sixty-one studies did not meet the inclusion criteria or were found to be duplicates, resulting in a total of 15 articles for analysis. Three articles were hand-searched. This comprehensive systematic review of the histopathology of HS confirms a high prevalence of follicular occlusion, follicular hyperkeratosis, and hyperplasia of the follicular epithelium. These findings support the central role of follicular occlusion in the development and progression of HS while providing a potential path to directing therapeutics against follicular occlusion.

化脓性汗腺炎(HS)是一种慢性炎症性瘢痕疾病,被认为与三叉区毛囊单位闭塞有关。我们对HS组织病理学进行了系统的回顾,以评估当前的知识和讨论未来的方向。检索PubMed和Scopus数据库,检索1985年1月至2021年1月发表的讨论HS病理的相关文章。其他文章通过手动检索确定,这需要手动扫描选定的期刊。在主要数据库的初步检索中,共确定了355条引文。在对标题、摘要和副本进行审查后,有279篇文章被排除在外。61项研究不符合纳入标准或发现重复,总共有15篇文章用于分析。有三篇文章是手工搜索的。本文对HS的组织病理学进行了全面系统的回顾,证实了滤泡闭塞、滤泡角化过度和滤泡上皮增生的高患病率。这些发现支持了滤泡阻塞在HS的发展和进展中的核心作用,同时为指导针对滤泡阻塞的治疗提供了潜在的途径。
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引用次数: 4
Cocaine/Levamisole-Induced, Skin-Limited ANCA-Associated Vasculitis with Pyoderma Gangrenosum-like Presentation. 可卡因/左旋咪唑诱导的皮肤局限性anca相关血管炎伴坏疽样脓皮病。
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-06-29 DOI: 10.3390/dermatopathology9030026
Mirjana Urosevic-Maiwald, Jan-Hendrik B Hardenberg, Jürg Hafner, Marie-Charlotte Brüggen

The use of levamisole as the most frequent adulterant of cocaine has merged in previously unknown toxicities, notably a disease entity called cocaine/levamisole-associated autoimmune syndrome (CLAAS). Clinically, CLAAS can manifest with diverse cutaneous and extracutaneous features sharing common laboratory findings (neutropenia, autoantibody patterns). We report the case of a cocaine-abusing female patient with relapsing episodes of painful ulcers, worsening and expanding over a three-year period. The case exhibited all features of a drug-induced, skin-limited, ANCA-associated vasculitis, evolving over time to PG-like findings. In both disease stages, the patient responded well to the cessation of cocaine exposure and systemic glucocorticosteroids. This case demonstrates the continuous nature of cutaneous CLAAS manifestations in a single patient. CLAAS has become a major public health issue in the at-risk group of cocaine users, and clinicians should be alert of this condition when treating cocaine users presenting with single or multiple skin ulcerations.

左旋咪唑作为可卡因最常见的掺假剂的使用已经合并了以前未知的毒性,特别是一种称为可卡因/左旋咪唑相关自身免疫综合征(CLAAS)的疾病实体。临床上,CLAAS可表现为多种皮肤和皮外特征,具有共同的实验室表现(中性粒细胞减少,自身抗体模式)。我们报告的情况下,可卡因滥用的女性患者复发发作疼痛的溃疡,恶化和扩大超过三年的时间。该病例表现出药物诱导、皮肤受限、anca相关血管炎的所有特征,随着时间的推移演变为pg样表现。在这两个疾病阶段,患者对停止可卡因暴露和全身糖皮质激素反应良好。本病例在单个患者中显示了皮肤CLAAS表现的连续性。CLAAS已成为高危可卡因使用者群体中的一个主要公共卫生问题,临床医生在治疗出现单一或多重皮肤溃疡的可卡因使用者时应警惕这种情况。
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引用次数: 0
Pseudo-Pemphigoid Gestationis Eruption Following SARS-CoV-2 Vaccination with mRNA Vaccine. 用mRNA疫苗接种SARS-CoV-2后的假类天疱疮妊娠爆发。
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-06-24 DOI: 10.3390/dermatopathology9030025
Caroline de Lorenzi, Gürkan Kaya, Laurence Toutous Trellu

Auto-immune reactions, including auto-immune bullous disease, have been reported following SARS-CoV-2 virus vaccination. Few cases of bullous pemphigoid are described, but there has been no case of pemphigoid gestationis. We report the first case here.

有报道称,在接种SARS-CoV-2病毒后会出现自身免疫反应,包括自身免疫性大疱病。很少有大疱性类天疱疮的病例被描述,但没有一例类天疱疮妊娠。我们在此报告第一例。
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引用次数: 2
Subungual Exostosis Presenting as a Pyogenic Granuloma-like Lesion with Reactive Myofibroblastic Proliferation in Two Young Women. 两名年轻女性的甲下外生骨肿表现为化脓性肉芽肿样病变,伴有反应性肌成纤维细胞增生。
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-06-20 DOI: 10.3390/dermatopathology9020024
Rosanna Fox, Effie Katsarma, Nick Tiffin, Manuraj Singh

Subungual exostosis (SE) is a well-recognised benign proliferation of the distal phalanx most often seen in young adults and affecting the big toe. Possible triggers include previous trauma and chronic irritation or infection. We describe two atypical cases of SE in two young women presenting with pyogenic granuloma-like lesions clinically. Diagnostic biopsies were performed to confirm the diagnosis and excluded amelanotic melanoma. However, histology unexpectedly revealed reactive myofibroblastic proliferations mimicking nodular fasciitis overlying the SE. Given the atypical clinical presentation, the diagnosis was initially missed or not considered in both patients. They highlight two important points; the first is that SEs may present with pyogenic granuloma-like lesions clinically and that histological analysis is then required to exclude malignancy, particularly amelanotic melanoma. Secondly, that the histology will show a reactive myofibroblastic proliferation and if the sample is relatively superficial and pathologists are not aware of this potential reaction pattern, the underlying diagnosis of SE may be missed.

趾骨下外生症(SE)是一种公认的远端指骨的良性增生,最常见于年轻人,影响大脚趾。可能的诱因包括以前的创伤和慢性刺激或感染。我们描述了两个不典型的病例SE在两名年轻女性表现为化脓性肉芽肿样病变的临床。进行诊断活检以确认诊断并排除无色素黑色素瘤。然而,组织学出乎意料地显示反应性肌成纤维细胞增生,类似结节性筋膜炎。鉴于非典型的临床表现,诊断最初被遗漏或没有考虑在两个病人。它们突出了两个要点;首先,se可能在临床上表现为化脓性肉芽肿样病变,需要进行组织学分析以排除恶性肿瘤,特别是无色素黑色素瘤。其次,组织学将显示反应性肌成纤维细胞增殖,如果样本相对肤浅,病理学家没有意识到这种潜在的反应模式,可能会错过SE的潜在诊断。
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引用次数: 0
Drug-Induced vs. Viral Maculopapular Exanthem—Resolving the Dilemma 药物致黄斑丘疹vs.病毒性黄斑丘疹:解决困境
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-05-07 DOI: 10.3390/dermatopathology9020021
S. Khandpur, R. Ahuja
Maculopapular exanthem is a commonly encountered presentation in routine clinical practice, and differentiation between its two most common etiologies, i.e., viral- and drug-induced, often poses a diagnostic dilemma. Clinical, hematological and biochemical investigations are seldom reliable in distinguishing between a drug reaction and a viral exanthem. Certain key histopathological features such as the presence of a moderate degree of spongiosis, extensive basal cell damage with multiple necrotic keratinocytes and dermal infiltrate rich in eosinophils or lymphocytes and histiocytes may favor a drug exanthem, while distinctive epidermal cytopathic changes and lymphocytic vasculitis point towards a viral etiology. Similarly, notable immunohistochemical markers such as IL-5, eotaxin and FAS ligand may support a diagnosis of a drug-induced maculopapular eruption. Histopathological and immunohistochemical evaluations may help in distinguishing between the two etiologies when faced with a clinical overlap, especially in patients on multiple essential drugs when drug withdrawal and rechallenge is not feasible.
黄斑丘疹是一种常见的临床表现,其两种最常见的病因,即病毒和药物引起的区分,往往造成诊断困境。临床、血液学和生化检查在区分药物反应和病毒检查方面很少可靠。某些关键的组织病理学特征,如存在中度海绵状病,广泛的基底细胞损伤伴多个坏死角质形成细胞和真皮浸润丰富的嗜酸性细胞或淋巴细胞和组织细胞,可能有利于药物检查,而明显的表皮细胞病变和淋巴细胞血管炎则指向病毒病因。同样,显著的免疫组织化学标志物如IL-5、eotaxin和FAS配体可能支持药物性黄斑丘疹的诊断。当面临临床重叠时,组织病理学和免疫组织化学评估可能有助于区分两种病因,特别是在需要多种基本药物且无法停药和重新挑战的患者中。
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引用次数: 2
Scar Endometriosis: A Rare Cause of Abdominal Pain 瘢痕性子宫内膜异位症:一种罕见的腹痛原因
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-05-05 DOI: 10.3390/dermatopathology9020020
R. Nepali, S. Upadhyaya Kafle, T. Pradhan, Jibanath Dhamala
Scar endometriosis or incisional endometriosis is the presence of endometrial tissues with glands in the previous incision or scar. Its overall estimated incidence after post-cesarean and post-hysterectomy is 0.03–0.4% and 1.08–2%, respectively. The patient presents with non-specific symptoms such as cyclical abdominal pain at the site of a previous surgical incision and scar and an abdominal lump with a cyclical increment in size, which is tender. The diagnosis is made only after the surgical excision with confirmation by histopathological analysis. We present the case of a 31-year-old female complaining of cyclical abdominal pain and a lump on the right side of a Pfannenstiel incision for five months. She had undergone two Lower Segment Caesarean Sections (LSCSs); the last surgery was eight months prior. Surgical excision was planned with the corresponding clinical features and radiological data. After the surgical excision, the sample was sent for histopathological examination, and scar endometriosis was diagnosed.
疤痕性子宫内膜异位症或切口性子宫内膜异位症是指在先前的切口或疤痕处存在腺体的子宫内膜组织。剖宫产后和子宫切除术后的总体估计发病率分别为0.03-0.4%和1.08-2%。患者表现出非特异性症状,如既往手术切口和疤痕部位周期性腹痛,腹部肿块周期性增大,触痛。只有在手术切除并经组织病理学分析证实后才能作出诊断。我们提出的情况下,31岁的女性抱怨周期性腹痛和肿块右侧的Pfannenstiel切口五个月。她接受了两次下段剖宫产术(LSCSs);上次手术是在八个月前。根据相应的临床特征和影像学资料计划手术切除。手术切除后送标本进行组织病理学检查,诊断为瘢痕性子宫内膜异位症。
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引用次数: 2
PRAME Expression as Helpful Immunohistochemical Marker in Rhabdoid Melanoma PRAME的表达作为有帮助的免疫组织化学标记物在横纹肌样黑色素瘤中的表达
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-05-02 DOI: 10.3390/dermatopathology9020019
V. Glutsch, M. Wobser, B. Schilling, A. Gesierich, M. Goebeler, H. Kneitz
Background: Rhabdoid melanoma is a rare variant of malignant melanoma with characteristic cytomorphologic features. Due to the potential loss of conventional melanocytic markers, histopathologic diagnosis is often challenging. We hypothesize that immunostaining for PReferentially expressed Antigen in MElanoma (PRAME) might have the potential to uncover the melanocytic origin of these dedifferentiated tumors. Methods: Four cases of rhabdoid primary melanomas were assessed by immunohistochemistry for expression of PRAME and conventional melanocytic markers. Immunohistochemical expression patterns were analyzed in the rhabdoid primaries and, if available, associated metastases. Results: All four cases of rhabdoid primary melanomas showed a strong nuclear positivity for PRAME, while the expression of conventional melanocytic markers S100, MART-1, SOX-10 and HMB-45 was variable between the analyzed cases. Conclusions: In summary, we report four cases of rhabdoid primary melanoma with high to intermediate expression of PRAME despite the partial and variable loss of other melanocytic markers. Hence, PRAME might facilitate the recognition of this highly aggressive entity to avoid misdiagnosis due to histopathologic pitfalls.
背景:横纹肌样黑色素瘤是一种罕见的恶性黑色素瘤变体,具有独特的细胞形态学特征。由于传统黑色素细胞标志物的潜在损失,组织病理学诊断往往具有挑战性。我们假设,黑色素瘤中PRAME参考表达抗原的免疫染色可能有可能揭示这些去分化肿瘤的黑色素细胞起源。方法:对4例横纹肌样原发性黑色素瘤进行免疫组化检测PRAME和常规黑色素细胞标志物的表达。对横纹肌样原发性肿瘤和相关转移瘤的免疫组织化学表达模式进行了分析。结果:所有四例横纹肌样原发性黑色素瘤均显示出PRAME的强核阳性,而传统黑色素细胞标志物S100、MART-1、SOX-10和HMB-45的表达在分析的病例之间是可变的。结论:总之,我们报告了四例横纹肌样原发性黑色素瘤,尽管其他黑色素细胞标志物部分和可变缺失,但PRAME高至中等表达。因此,PRAME可能有助于识别这种高度侵袭性的实体,以避免由于组织病理学陷阱而导致的误诊。
{"title":"PRAME Expression as Helpful Immunohistochemical Marker in Rhabdoid Melanoma","authors":"V. Glutsch, M. Wobser, B. Schilling, A. Gesierich, M. Goebeler, H. Kneitz","doi":"10.3390/dermatopathology9020019","DOIUrl":"https://doi.org/10.3390/dermatopathology9020019","url":null,"abstract":"Background: Rhabdoid melanoma is a rare variant of malignant melanoma with characteristic cytomorphologic features. Due to the potential loss of conventional melanocytic markers, histopathologic diagnosis is often challenging. We hypothesize that immunostaining for PReferentially expressed Antigen in MElanoma (PRAME) might have the potential to uncover the melanocytic origin of these dedifferentiated tumors. Methods: Four cases of rhabdoid primary melanomas were assessed by immunohistochemistry for expression of PRAME and conventional melanocytic markers. Immunohistochemical expression patterns were analyzed in the rhabdoid primaries and, if available, associated metastases. Results: All four cases of rhabdoid primary melanomas showed a strong nuclear positivity for PRAME, while the expression of conventional melanocytic markers S100, MART-1, SOX-10 and HMB-45 was variable between the analyzed cases. Conclusions: In summary, we report four cases of rhabdoid primary melanoma with high to intermediate expression of PRAME despite the partial and variable loss of other melanocytic markers. Hence, PRAME might facilitate the recognition of this highly aggressive entity to avoid misdiagnosis due to histopathologic pitfalls.","PeriodicalId":42885,"journal":{"name":"Dermatopathology","volume":"9 1","pages":"148 - 157"},"PeriodicalIF":1.9,"publicationDate":"2022-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42188972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Primary Cutaneous Gamma-Delta T-Cell Lymphoma Initially Diagnosed as Subcutaneous Panniculitis-like T-Cell Lymphoma with Dermatomyositis 原发性皮肤γ - δ t细胞淋巴瘤最初诊断为皮下泛膜炎样t细胞淋巴瘤伴皮肌炎
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-04-29 DOI: 10.3390/dermatopathology9020018
Chika Hirata, K. Nakai, Yusuke Kurasawa, N. Maekawa, S. Kuniyuki, K. Yamagami, M. Ohsawa, D. Tsuruta
Primary cutaneous gamma-delta T-cell lymphoma (CGD-TCL) is a rare cutaneous lymphoma. Panniculitis-like T-cell lymphoma (SPTCL) has a better prognosis than CGD-TCL. SPTCL is sometimes associated with autoimmune disease. A 64-year-old Japanese female with a history of dermatomyositis presented with subcutaneous nodules on the upper extremities and exacerbated dermatomyositis. A skin biopsy showed lobular panniculitis, a vacuolar interface change, and a dermal mucin deposit. Fat cells rimmed by neoplastic cells, fat necrosis, and karyorrhexis were observed. The atypical lymphoid cells showed CD3+, CD4−, CD8+, granzyme B+, CD20−, and CD56−. Polymerase chain reaction analysis demonstrated a T-cell receptor rearrangement. The patient was initially diagnosed with SPTCL, so the dose of prednisone was raised from 7.5 to 50 mg daily (1 mg/kg). After one month, erythematous nodules regressed, and muscle symptoms improved. Subsequently, prednisone was tapered, and cyclosporin A was added. After one year, the patient remained symptom-free and continued taking 7.5 mg prednisone and 100 mg cyclosporin A daily. Afterward, we immunostained skin samples with antibodies against TCR-ß and δ and found positive TCR-δ and negative TCR-ß. Therefore, we corrected the diagnosis to CGD-TCL, although the clinical course and the presence of dermatomyositis were reminiscent of SPTCL.
原发性皮肤γ δ t细胞淋巴瘤(CGD-TCL)是一种罕见的皮肤淋巴瘤。Panniculitis-like T-cell lymphoma (SPTCL)预后优于CGD-TCL。SPTCL有时与自身免疫性疾病有关。一名64岁日本女性,有皮肌炎病史,上肢皮下结节,皮肌炎加重。皮肤活检显示小叶性绒毛炎、空泡界面改变和真皮粘蛋白沉积。观察到脂肪细胞被肿瘤细胞包围,脂肪坏死,核裂。非典型淋巴样细胞表现为CD3+、CD4−、CD8+、颗粒酶B+、CD20−和CD56−。聚合酶链反应分析证实t细胞受体重排。患者最初被诊断为SPTCL,因此强的松剂量从每天7.5 mg增加到50 mg (1 mg/kg)。1个月后,红斑结节消退,肌肉症状改善。随后,泼尼松逐渐减少,并加入环孢素A。一年后,患者仍无症状,继续每天服用7.5 mg强的松和100 mg环孢素A。随后,我们用抗TCR- β和δ抗体对皮肤样本进行免疫染色,发现TCR-δ阳性,TCR- β阴性。因此,我们将诊断纠正为CGD-TCL,尽管临床病程和皮肌炎的存在令人联想到SPTCL。
{"title":"Primary Cutaneous Gamma-Delta T-Cell Lymphoma Initially Diagnosed as Subcutaneous Panniculitis-like T-Cell Lymphoma with Dermatomyositis","authors":"Chika Hirata, K. Nakai, Yusuke Kurasawa, N. Maekawa, S. Kuniyuki, K. Yamagami, M. Ohsawa, D. Tsuruta","doi":"10.3390/dermatopathology9020018","DOIUrl":"https://doi.org/10.3390/dermatopathology9020018","url":null,"abstract":"Primary cutaneous gamma-delta T-cell lymphoma (CGD-TCL) is a rare cutaneous lymphoma. Panniculitis-like T-cell lymphoma (SPTCL) has a better prognosis than CGD-TCL. SPTCL is sometimes associated with autoimmune disease. A 64-year-old Japanese female with a history of dermatomyositis presented with subcutaneous nodules on the upper extremities and exacerbated dermatomyositis. A skin biopsy showed lobular panniculitis, a vacuolar interface change, and a dermal mucin deposit. Fat cells rimmed by neoplastic cells, fat necrosis, and karyorrhexis were observed. The atypical lymphoid cells showed CD3+, CD4−, CD8+, granzyme B+, CD20−, and CD56−. Polymerase chain reaction analysis demonstrated a T-cell receptor rearrangement. The patient was initially diagnosed with SPTCL, so the dose of prednisone was raised from 7.5 to 50 mg daily (1 mg/kg). After one month, erythematous nodules regressed, and muscle symptoms improved. Subsequently, prednisone was tapered, and cyclosporin A was added. After one year, the patient remained symptom-free and continued taking 7.5 mg prednisone and 100 mg cyclosporin A daily. Afterward, we immunostained skin samples with antibodies against TCR-ß and δ and found positive TCR-δ and negative TCR-ß. Therefore, we corrected the diagnosis to CGD-TCL, although the clinical course and the presence of dermatomyositis were reminiscent of SPTCL.","PeriodicalId":42885,"journal":{"name":"Dermatopathology","volume":"9 1","pages":"143 - 147"},"PeriodicalIF":1.9,"publicationDate":"2022-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47733979","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Conceptual Evolution and Current Approach to Spitz Tumors Spitz肿瘤的概念演变和目前的研究方法
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-04-26 DOI: 10.3390/dermatopathology9020017
C. Urso, V. de Giorgi, D. Massi
Over the past several decades, the study of Spitz neoplasms has flourished, with expanded conceptualization and refined terminology, providing a framework for the assessment and classification of Spitz nevi, atypical Spitz Tumors, and Spitz melanoma. Cancer genomics have generated concepts such as driver and passenger genes and clonal evolution, which can be applied to Spitz tumors. Herein, we provide a historical perspective, followed by a summary of current knowledge and clinical approaches for these challenging tumors.
在过去的几十年里,Spitz肿瘤的研究蓬勃发展,随着概念的扩展和术语的完善,为Spitz痣、非典型Spitz肿瘤和Spitz黑色素瘤的评估和分类提供了一个框架。癌症基因组学已经产生了诸如驱动基因和乘客基因以及克隆进化等概念,这些概念可以应用于Spitz肿瘤。在这里,我们提供了一个历史的观点,其次是当前的知识和临床方法的总结,这些具有挑战性的肿瘤。
{"title":"Conceptual Evolution and Current Approach to Spitz Tumors","authors":"C. Urso, V. de Giorgi, D. Massi","doi":"10.3390/dermatopathology9020017","DOIUrl":"https://doi.org/10.3390/dermatopathology9020017","url":null,"abstract":"Over the past several decades, the study of Spitz neoplasms has flourished, with expanded conceptualization and refined terminology, providing a framework for the assessment and classification of Spitz nevi, atypical Spitz Tumors, and Spitz melanoma. Cancer genomics have generated concepts such as driver and passenger genes and clonal evolution, which can be applied to Spitz tumors. Herein, we provide a historical perspective, followed by a summary of current knowledge and clinical approaches for these challenging tumors.","PeriodicalId":42885,"journal":{"name":"Dermatopathology","volume":"9 1","pages":"136 - 142"},"PeriodicalIF":1.9,"publicationDate":"2022-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43420091","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
“Lichenoid Granulomatous Pattern” in a Case of Lupus Vulgaris 一例寻常型狼疮的“地衣样肉芽肿型”
IF 1.9 Q3 DERMATOLOGY Pub Date : 2022-04-20 DOI: 10.3390/dermatopathology9020016
C. Desai, Ismail Shaikh
Lupus vulgaris is a one of the most common skin infections in the Indian subcontinent. Even today, it often creates a diagnostic dilemma for both clinicians and histopathologists. We describe a case of lupus vulgaris that showed lichenoid granulomatous inflammation in the dermis. This pattern is not uncommon, but is rarely described in the literature as newer modalities currently take precedence in diagnosis. Our aim is to make clinicians and dermatopathologists aware of this pattern of inflammation seen in this common infection.
寻常性狼疮是印度次大陆最常见的皮肤感染之一。即使在今天,它也经常给临床医生和组织病理学家造成诊断困境。我们描述了一个寻常狼疮的情况下,显示苔藓样肉芽肿炎症在真皮。这种模式并不罕见,但在文献中很少描述,因为目前较新的模式优先于诊断。我们的目的是使临床医生和皮肤病理学家意识到这种常见感染中所见的炎症模式。
{"title":"“Lichenoid Granulomatous Pattern” in a Case of Lupus Vulgaris","authors":"C. Desai, Ismail Shaikh","doi":"10.3390/dermatopathology9020016","DOIUrl":"https://doi.org/10.3390/dermatopathology9020016","url":null,"abstract":"Lupus vulgaris is a one of the most common skin infections in the Indian subcontinent. Even today, it often creates a diagnostic dilemma for both clinicians and histopathologists. We describe a case of lupus vulgaris that showed lichenoid granulomatous inflammation in the dermis. This pattern is not uncommon, but is rarely described in the literature as newer modalities currently take precedence in diagnosis. Our aim is to make clinicians and dermatopathologists aware of this pattern of inflammation seen in this common infection.","PeriodicalId":42885,"journal":{"name":"Dermatopathology","volume":"9 1","pages":"131 - 135"},"PeriodicalIF":1.9,"publicationDate":"2022-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44182967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Dermatopathology
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