Primary cutaneous leiomyosarcoma of the flank: Case report and review

IF 0.2 Q4 DERMATOLOGY
J. Ben Hassouna , F. Saadallah , B. Mezghani , M. Ali Ayedi , L. Charfi , L. Achouri , T. Dhieb , K. Rahal
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引用次数: 2

Abstract

Cutaneous leiomyosarcoma is a rare soft tissue sarcoma. We present a case of a 50-year-old man, with a rare location in the flank. Clinical presentation showed an ulcerative lesion. Imaging features were evocative of malignancy. Surgical excision was performed, involving oblique muscles. The diagnosis of low-grade leiomyosarcoma with free margins was made. No adjuvant therapy was indicated. Clinical and radiological follow-up of the patient during two years did not reveal recurrences. Cutaneous leiomyosarcoma of the flank is extremely rare and takes part in a group of infrequent and unknown tumors. Clinical presentation is unspecific and histological evidence is mandatory for diagnosis. Tumor extension in depth constitutes the major determinant factor for therapeutic management and prognosis. Wide surgical resection is crucial to minimize recurrence risk especially when poor prognostic factors take place.

原发性腹部皮肤平滑肌肉瘤:病例报告与回顾
摘要皮肤平滑肌肉瘤是一种罕见的软组织肉瘤。我们报告一个50岁男性的病例,在侧翼有一个罕见的位置。临床表现为溃疡性病变。影像学特征提示恶性肿瘤。手术切除,包括斜肌。诊断为低级别平滑肌肉瘤伴游离缘。无辅助治疗。两年的临床和放射学随访均未发现复发。腹侧皮肤平滑肌肉瘤极为罕见,是一组罕见且未知的肿瘤。临床表现不明确,组织学证据是诊断的必要依据。肿瘤的深度扩展是治疗管理和预后的主要决定因素。广泛的手术切除是减少复发风险的关键,尤其是在预后不良的情况下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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