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踝关节毛母质瘤:一例报告

Pilomatrixoma of the Ankle: A Case Report.

作者信息

Ahmed Sayed Mohamed S

机构信息

College of Medicine, I.M. Sechenov First Moscow State Medical University, Moscow, RUS.

出版信息

Cureus. 2024 Jul 10;16(7):e64238. doi: 10.7759/cureus.64238. eCollection 2024 Jul.

Abstract

Pilomatrixoma, also known as calcifying epithelioma of Malherbe, is a rare benign skin tumor originating from hair follicle matrix cells. It typically presents as a firm, painless subcutaneous nodule, most commonly found in the head, neck, and upper extremities. Pilomatrixoma can occasionally appear in atypical locations, posing a diagnostic challenge due to its nonspecific clinical presentation. A 43-year-old female presented with a painless, slowly enlarging mass on the lateral side of her left ankle, which had been present for approximately one year. Physical examination revealed a firm, well-circumscribed subcutaneous nodule measuring about 2 cm in diameter with normal overlying skin. An MRI of the left ankle demonstrated a well-circumscribed, subcutaneous mass with heterogeneous signal intensity, consistent with calcifications, suggesting pilomatrixoma. A fine-needle aspiration biopsy confirmed the presence of basaloid cells, shadow cells, and areas of calcification. The lesion was surgically excised, and histopathological examination validated the diagnosis of pilomatrixoma. The patient had an uneventful postoperative course, with no recurrence at the six-month follow-up. This case underscores the importance of considering pilomatrixoma in the differential diagnosis of subcutaneous nodules, even in unusual locations. A comprehensive diagnostic approach, including clinical evaluation, imaging, and histopathological examination, is essential for an accurate diagnosis. Surgical excision with clear margins is the treatment of choice, ensuring low recurrence rates and excellent patient outcomes. This report enhances the understanding of pilomatrixoma and highlights the necessity for a multimodal diagnostic strategy in managing this rare condition effectively.

摘要

毛母质瘤,也称为马尔赫布钙化上皮瘤,是一种罕见的起源于毛囊基质细胞的良性皮肤肿瘤。它通常表现为一个坚实、无痛的皮下结节,最常见于头部、颈部和上肢。毛母质瘤偶尔会出现在非典型部位,因其非特异性临床表现而带来诊断挑战。一名43岁女性,左踝外侧出现一个无痛、缓慢增大的肿块,已存在约一年。体格检查发现一个直径约2厘米、边界清晰的坚实皮下结节,其上覆盖的皮肤正常。左踝的磁共振成像显示一个边界清晰的皮下肿块,信号强度不均匀,符合钙化表现,提示为毛母质瘤。细针穿刺活检证实存在基底样细胞、影细胞及钙化区域。该病变经手术切除,组织病理学检查证实为毛母质瘤。患者术后恢复顺利,六个月随访时无复发。该病例强调了即使在不寻常部位的皮下结节鉴别诊断中考虑毛母质瘤的重要性。包括临床评估、影像学检查和组织病理学检查在内的综合诊断方法对于准确诊断至关重要。手术切除切缘清晰是首选治疗方法,可确保低复发率并取得良好的患者预后。本报告增进了对毛母质瘤的理解,并强调了采用多模式诊断策略有效管理这种罕见疾病的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a1/11313151/f78ce83fa72e/cureus-0016-00000064238-i01.jpg

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