Yalçın Özben, Aygün Mine İlayda Şengör, Moustafa Elif, Aktaş Ezgi
Department of Pathology.
Department of Dermatology, Prof Dr. Cemil Taşcıoğlu City Hospital, Istanbul, Turkey.
Dermatol Reports. 2024 Feb 6;16(3):9915. doi: 10.4081/dr.2024.9915. eCollection 2024 Sep 2.
Morphea is a rare autoimmune disease that often affects skin and subcutaneous tissues. The aim of this study was to determine the association between patient demographic parameters, lesion site, clinical subtype of morphea, and histological findings. Between 2016 and 2022, we investigated 78 patients with morphea at the Department of Pathology, Prof. Dr. Cemil Taşcıoğlu City Hospital in Turkey. Case-specific hematoxylin and eosin stain slides were obtained from the pathology archive and assessed blindly by two pathologists. 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 SPSS Statistics v.20 (IBM, Armonk, NY, USA). The most common clinical presentation was plaque type (87.5%), while histopathological findings included homogenization of dermal collagen (100%) and decrease of skin appendages (98.7%). Flattening of the rete ridges was observed in 46.2% of patients. Severity of the inflammatory infiltrate was found to be higher in these patients (p=0.028). Basal pigmentation was observed in 59% of patients. sign was more common in lower extremity lesions among all localizations (p=0.015). 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 sign could be helpful for identifying lesions located in the lower extremities.
硬斑病是一种罕见的自身免疫性疾病,常累及皮肤和皮下组织。本研究的目的是确定患者人口统计学参数、病变部位、硬斑病临床亚型和组织学结果之间的关联。2016年至2022年期间,我们在土耳其杰米尔·塔什乔奥卢市立医院病理科对78例硬斑病患者进行了调查。从病理档案中获取特定病例的苏木精和伊红染色切片,并由两名病理学家进行盲法评估。评估了 rete 嵴的变平、炎症浸润的位置、炎症浸润的程度、浆细胞的存在、嗜酸性粒细胞的存在、真皮胶原的均质化、皮肤附属器的减少、基底色素沉着和黑色素失禁。使用SPSS Statistics v.20(美国纽约州阿蒙克市IBM公司)进行统计分析。最常见的临床表现为斑块型(87.5%),而组织病理学结果包括真皮胶原的均质化(100%)和皮肤附属器的减少(98.7%)。46.2%的患者观察到 rete 嵴变平。这些患者的炎症浸润严重程度更高(p=0.028)。59%的患者观察到基底色素沉着。在所有部位中, 征在下肢病变中更常见(p=0.015)。硬斑病的组织病理学特征多变且令人困惑。特别是,在胶原均质化的病例中,应结合临床进行鉴别诊断时考虑硬斑病。此外, 征可能有助于识别位于下肢的病变。