罕见的皮肤纤维瘤合并溃疡1例报告。

IF 1.7 Q3 DERMATOLOGY
Lamia Alakrash, Renad AlKanaan, Rema Aldihan, Alanoud Alsuhibani, Salman Almalki
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引用次数: 0

摘要

皮肤纤维瘤是一种常见的间质皮肤病变,典型表现为坚硬、生长缓慢的结节。通常,这种病变是无症状的;然而,在某些情况下,它们也会引起不适。溃疡是皮肤纤维瘤的罕见特征,在这种情况下诊断往往是困难的。我们报告一例67岁的女性,患有多种合并症,包括胰腺癌,接受新辅助化疗,因急性肺栓塞入院。患者表现为偶然的大腿内侧病变。病变无症状,溃烂,一个月前渗出脓。临床检查显示溃疡深3 × 2 cm,边缘凹陷,基底干燥黄白色,边缘呈紫色。组织病理学证实皮肤纤维瘤伴表皮增生、真皮梭形细胞增生、组织细胞和胶原陷住。免疫组化CD68、CD10、因子XIII阳性。由于病人病情恶化,没有对她进行干预,她死于原发疾病。该病例的独特之处在于其在复杂全身性疾病患者中的非典型溃疡表现,并强调区分良性病变和恶性病变,特别是在临床表现不明确的病例中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Unusual Presentation of Dermatofibroma with Ulcer: A Case Report.

Dermatofibroma is a common mesenchymal skin lesion that typically presents as a firm, slow-growing nodule. Generally, such lesions are asymptomatic; however, they can also cause discomfort in some cases. Ulceration is an uncommon feature of dermatofibroma, and diagnosis in such cases is often difficult. We report a case of a 67-year-old female with multiple comorbidities, including pancreatic cancer undergoing neoadjuvant chemotherapy, who was admitted for acute pulmonary embolism. The patient presented with an incidental medial thigh lesion. The lesion was asymptomatic, ulcerated, and oozing pus one month before presentation. Clinical examination revealed a 3 × 2 cm deep ulcer with a punched-out edge, a dry yellow-white base, and a firm violaceous border. Histopathology confirmed dermatofibroma with epidermal hyperplasia, dermal spindle cell proliferation, histiocytes, and collagen trapping. Immunohistochemistry was positive for CD68, CD10, and Factor XIII. Due to the deteriorating condition of the patient, no intervention was provided to her, and she succumbed to her primary illness. This case is unique due to its atypical ulcerative presentation in a patient with complex systemic illness and emphasizes distinguishing between benign lesions and malignant mimics, especially in cases which have ambiguous clinical presentation.

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来源期刊
Dermatopathology
Dermatopathology DERMATOLOGY-
自引率
5.30%
发文量
39
审稿时长
11 weeks
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