A Case of Digital Intraosseous Epidermoid Inclusion Cyst of the Distal Phalanx

S. Hwang
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Abstract

Intraosseous epidermoid inclusion cyst is a very rare cystic lesion of the bone, that has been reported primarily in middle-aged men. A congenital etiology has been proposed, although post-traumatic or iatrogenic events remain the most prevalent hypotheses. A 61-year-old woman visited Soonchunhyang University Gumi Hospital complaining of painful swelling of her right middle finger. Radiologic findings of the lesion showed a well-defined, lytic, expansile lesion originating at the tip of the distal phalanx. Preoperative imaging suggested benign cartilage tumors such as enchondroma or acute osteomyelitis. Intralesional curettage, culture, and biopsy were performed. Histopathological analysis demonstrated stratified squamous epithelium with keratinized cellular debris, consistent with a diagnosis of digital intraosseous epidermoid inclusion cyst. We present a case of an epidermoid inclusion cyst originating at the tip of the distal phalanx of the right middle finger.
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指骨远端指骨内表皮样包涵囊肿1例
骨内表皮样包涵囊肿是一种非常罕见的骨囊性病变,主要发生于中年男性。虽然创伤后或医源性事件仍然是最普遍的假设,但已提出先天性病因。顺天乡大学龟尾医院的A某(61岁)表示,右手中指肿痛。病灶的放射学表现为一清晰、溶解性、扩张性病灶,起源于远节指骨尖端。术前影像学提示为良性软骨肿瘤,如软骨瘤或急性骨髓炎。进行病灶内刮除、培养和活检。组织病理学分析显示层状鳞状上皮伴角化细胞碎片,符合指骨内表皮样包涵性囊肿的诊断。我们报告一例起源于右中指远端指骨尖端的表皮样包涵囊肿。
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