Perforating granuloma annulare mimicking keratoacanthoma: A case report

Dilek Menteşoğlu, H. Khurami, A. Karaduman, Ö. Gököz
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Abstract

Perforating granuloma annulare (PGA) is a infrequent type of granuloma annulare. PGA has a chronic course. The etiology and perforation mechanism are still obscure. We submit a case of a 32-year-old male patient who presented with a 2-month history of asymptomatic lesion on the dorsum of his hand. He did not report the use of any medication, infection, vaccine, trauma, autoimmune disorders, heart disease, and malignancy. Complete blood count, thyroid function tests, lipid profile parameters, and fasting blood glucose were within normal ranges. Moreover, the human immunodeficiency virüs was negative. Histopathologic examination revealed that accumulation of mucin was at the center of the histiocytic reaction, which was grouped in places. Therefore, we diagnosed PGA with clinical and histopathological data. The presented case emphasizes that PGA should be considered in the differential diagnosis of keratotic/ umbilical papules on the dorsum of the hand.
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模拟角棘肿的环形穿孔肉芽肿1例
穿孔性环形肉芽肿是一种少见的环形肉芽肿。PGA有慢性病程。病因和穿孔机制仍不清楚。我们报告一个32岁的男性患者,他的手背有2个月的无症状病变史。他没有报告使用任何药物、感染、疫苗、创伤、自身免疫性疾病、心脏病和恶性肿瘤。全血细胞计数、甲状腺功能检查、血脂参数和空腹血糖均在正常范围内。此外,人类免疫缺陷病毒 s为阴性。组织病理学检查显示,黏液积聚在组织细胞反应的中心,并呈成组分布。因此,我们根据临床和组织病理学资料诊断PGA。本病例强调PGA在手背角化/脐丘疹的鉴别诊断中应予以考虑。
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