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三例巨大毛母质瘤——对上半身存在大量内部钙化的巨大皮肤肿瘤的诊断和治疗的思考。

Three cases of giant pilomatrixoma--considerations for diagnosis and treatment of giant skin tumours with abundant inner calcification present on the upper body.

机构信息

Department of Plastic and Reconstructive Surgery, Hakodate Goryokaku Hospital, 38-3 Goryokaku-cho, Hakodate 040-8611, Japan.

出版信息

J Plast Reconstr Aesthet Surg. 2010 Jun;63(6):e519-24. doi: 10.1016/j.bjps.2009.12.006. Epub 2010 Jan 18.

Abstract

BACKGROUND

Pilomatrixoma frequently occurs as a solitary, small tumour on the face or upper extremities of people younger than 20 years.

METHODS

We report three cases of giant pilomatrixoma. In all these cases, outward appearances and imaging investigations suggested malignant tumours. Preoperative biopsies suggested that case 1 was a basal cell carcinoma, but cases 2 and 3 had no malignant features on biopsy. Two of the cases experienced rare complications - hypercalcaemia caused by parathyroid-related protein (PTHrP) production and multiple occurrences.

RESULTS

All three tumours were removed with a 1-3-cm margin. The postoperative histopathologies showed pilomatrixoma in all three cases.

CONCLUSIONS

Rarely, pilomatrixoma develops to a giant size with various atypical outward appearances consistent with a malignant tumour. Preoperative clinical appearances frequently lead to misdiagnosis, and preoperative examinations are unreliable. Therefore, when a giant tumour with abundant inner calcification is present in a young patient, the possibility of a pilomatrixoma should be considered.

摘要

背景

毛母质瘤常作为发生于 20 岁以下人群面部或上肢的单发、小肿瘤出现。

方法

我们报告了 3 例巨大毛母质瘤。所有这些病例的外观和影像学检查均提示为恶性肿瘤。术前活检提示例 1 为基底细胞癌,但例 2 和例 3 的活检无恶性特征。其中 2 例出现罕见并发症——由甲状旁腺相关蛋白(PTHrP)产生引起的高钙血症和多次发作。

结果

所有 3 例肿瘤均以 1-3cm 的切缘切除。术后组织病理学检查显示 3 例均为毛母质瘤。

结论

罕见情况下,毛母质瘤可发展为具有多种非典型外观的巨大肿瘤,类似于恶性肿瘤。术前临床表现常导致误诊,术前检查不可靠。因此,当年轻患者存在富含内部钙化的巨大肿瘤时,应考虑毛母质瘤的可能性。

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