原发性面部皮肤平滑肌肉瘤:一种难以诊断的罕见肿瘤

Bakary Ouattara, Konan Marc Koffi, Ory Opokou Alexandre Demisère, Koffi Laurent Boka, Rokiatou Kone, Aké Lucien Jonathan Yapo, Assoumou Lucien Asseke, Mouan Beatrice Harding, Pierre Breton
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引用次数: 0

摘要

平滑肌肉瘤是一种罕见的下肢恶性肿瘤。它的鉴别组织学诊断是困难的,并且在存在年轻的疤痕组织,平滑肌瘤,皮肤纤维瘤,黑色素瘤,rabdomyosarcoma,肉瘤样癌,纤维黄色瘤,Darrier Ferrand皮肤纤维肉瘤和肌纤维母细胞肿瘤时进行诊断。治疗基本上是手术,手术边缘为3至5厘米。我们报告了两个局部肿瘤的观察结果,包括一个已知的平滑肌肉瘤病例和另一个最初诊断为平滑肌肉瘤的病例,经过几次读数后,结果证明是细胞肌纤维瘤,没有恶性肿瘤的迹象。这项工作的目的是回顾文献对这种病理,同时突出诊断和治疗的困难。结论:平滑肌肉瘤是一种罕见的平滑肌肿瘤,在治疗不完全的情况下,局部复发的风险很高,其真皮部分的平滑肌肉瘤优先位于头颈部。它的治疗完全是外科手术和高度致残。
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Primary Cutaneous Leiomyosarcoma of the Face: A Rare Tumor that Is Difficult to Diagnose
Leiomyosarcoma is a rare malignant tumour of the lower limbs. Its differential histological diagnosis is difficult and is made in the presence of young scar tissue, leimyoma, dermatofibroma, melanoma, rabdomyosarcoma, sarcomatoid carcinoma, fibroxantoma, Darrier Ferrand dermatofibrosarcoma and myofibroblastic tumours. Treatment is essentially surgical, with margins of 3 to 5 centimetres. We report two observations of tumours localised to the face, including one case of a known leiomyosarcoma and another case initially diagnosed as a leiomyosarcoma which turned out to be a cellular myofibroma with no sign of malignancy after several readings. The aim of this work is to review the literature on this pathology while highlighting the diagnostic and therapeutic difficulties. Conclusion: A rare smooth muscle tumour with a high risk of local recurrence in the event of incomplete treatment, leiomyosarcoma in its dermal component is preferentially located in the head and neck. Its treatment is exclusively surgical and highly mutilating.
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