Histopathologic spectrum of morphea: a single-center retrospective study

IF 2.3 Q2 DERMATOLOGY Dermatology Reports Pub Date : 2024-02-06 DOI:10.4081/dr.2024.9915
Ö. Yalçın, Mine İlayda Şengör Aygün, Elif Moustafa, Ezgi Aktaş
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Abstract

Background. Morphea is a rare autoimmune disease that often affects the skin and subcutaneous tissue. Objective. The aim of our study is to reveal the relationship between demographic characteristics of the patients, location of the lesions, clinical subtype of morphea and histopathological findings. Methods. We studied 78 patients diagnosed with morphea between 2016 and 2022 at the Department of Pathology, Prof. Dr. Cemil Taşcıoğlu City Hospital. 72 patients were included in the study. Hematoxylin and Eosin stain slides of cases were retrieved from the pathology archive and were evaluated by two pathologists under blinded conditions. Flattening of rete ridges, location of inflammatory infiltrate, grade of inflammatory infiltrate, presence of plasma cells, presence of eosinophils, homogenization of dermal collagen, decrease of skin appendages, basal pigmentation and melanin incontinence were evaluated. Statistical analyses were performed using SPSSv.20. Results. The most common clinical presentation was plaque type(87.5%) and histopathological findings were homogenization of dermal collagen(100%) and decrease of skin appendages (98.7%). Flattening of the rete ridges was observed in 46.2% of the patients. Severity of the inflammatory infiltrate was found to be higher in these patients(p=0.028). Basal pigmentation was observed in 59% of the patients. Line sign was more common in lower extremity lesions among all localizations (p=0.015). Conclusions. The histopathologic features of morphea are variable and confusing. Particularly, in cases with collagen homogenization, morphea should be considered in differential diagnosis with clinical correlation. In addition, the ‘line’ sign could be helpful for identifying lesions located in the lower extremities.
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白斑病的组织病理学谱:一项单中心回顾性研究
背景。莫泊桑是一种罕见的自身免疫性疾病,通常会影响皮肤和皮下组织。研究目的我们的研究旨在揭示患者的人口统计学特征、皮损部位、灰斑病的临床亚型和组织病理学结果之间的关系。研究方法我们研究了2016年至2022年期间在Cemil Taşcıoğlu市医院病理科确诊的78名莫非格氏病患者。研究共纳入 72 名患者。病例的血色素和伊红染色切片取自病理档案,由两名病理学家在盲法条件下进行评估。评估内容包括齿脊变平、炎症浸润的位置、炎症浸润的等级、浆细胞的存在、嗜酸性粒细胞的存在、真皮胶原的均质化、皮肤附属物的减少、基底色素沉着和黑色素失禁。使用 SPSSv.20 进行统计分析。结果最常见的临床表现为斑块型(87.5%),组织病理学结果为真皮胶原均质化(100%)和皮肤附属物减少(98.7%)。46.2%的患者可观察到齿嵴变平。这些患者的炎症浸润程度较高(P=0.028)。59%的患者出现基底色素沉着。在所有病变部位中,线状征在下肢病变中更为常见(P=0.015)。结论白斑病的组织病理学特征多变且容易混淆。特别是在胶原匀质化的病例中,应结合临床相关性考虑病变的鉴别诊断。此外,"线 "征也有助于识别位于下肢的病变。
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来源期刊
Dermatology Reports
Dermatology Reports DERMATOLOGY-
CiteScore
1.40
自引率
0.00%
发文量
74
审稿时长
10 weeks
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