Cutaneous and subcutaneous leiomyosarcoma. A clinicopathologic study of 47 patients.

Pathologia Europaea Pub Date : 1974-01-01
I Dahl, L Angervall
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Abstract

A retrospective study of 47 patients with leiomyosarcoma of superficial (skin and subcutaneous) soft tissue is presented. The criteria for the light microscopic diagnosis are given and the differential diagnoses are discussed. Forty patients had a solitary tumour which, in 19 patients, was situated entirely or almost entirely in the corium. There were two distinct growth patterns for the leiomyosarcomas. The cutaneous tumours were poorly delimited and the subcutaneous tumours more well-circumscribed or nodular. Some three quarters of the tumours were located in the extremities, the thigh and hip regions being the predilection sites; the highest frequency was noted in patients in their seventies; the ages ranged between 25 and 89 years. The sex ratio (male to female) was 2 to 1. In 37 patients follow-up information was available, the follow-up period ranging from 1 month to 16 1/2 years; the median time was 6 years. One or more local recurrences developed in 15 patients. Seven out of the 47 patients had multiple leiomyosarcomas; 4 of these patients had already been operated on for a retroperitoneal leiomyosarcoma. Fourteen patients in the whole series died with metastases especially in the lungs. Metastases were seen particularly in patients with subcutaneous and multiple leiomyosarcomas. Our study suggest that the size and the mitotic activity of the tumour appear to have some prognostic value. The initial surgical procedure was found to be the most important factor in influencing the outcome of the disease and it is stressed that leiomyosarcoma in superficial soft tissues should be treated by wide surgical excision. It is recommended that patients with multiple leiomyosarcomas in the superficial soft tissues should be subjected to further examination in order to exclude the possible occurrence of a retroperitoneal tumour. Finally, we consider that the use of a trichrome stain, such as the haematoxylin-van Gieson's stain, is superior to the haematoxylin-eosin stain in diagnosing leiomyosarcoma.

皮肤和皮下平滑肌肉瘤。47例患者的临床病理分析。
本文对47例浅表(皮肤及皮下)软组织平滑肌肉瘤进行回顾性研究。给出了光镜诊断标准,并对鉴别诊断进行了讨论。40名患者有一个孤立的肿瘤,其中19名患者完全或几乎完全位于核芯。平滑肌肉瘤有两种不同的生长模式。皮肤肿瘤界限模糊,皮下肿瘤界限清晰或呈结节状。大约四分之三的肿瘤位于四肢,大腿和臀部区域是偏爱的部位;70多岁的患者出现频率最高;年龄在25岁到89岁之间。男女性别比为2:1。37例患者有随访资料,随访时间从1个月到16年半不等;平均时间为6年。15例患者出现一次或多次局部复发。47例患者中有7例患有多发性平滑肌肉瘤;其中4例患者已因腹膜后平滑肌肉瘤接受手术治疗。整个系列中有14例患者死于转移,尤其是肺转移。转移尤其见于皮下和多发性平滑肌肉瘤患者。我们的研究表明,肿瘤的大小和有丝分裂活性似乎有一定的预后价值。最初的外科手术是影响疾病预后的最重要因素,强调浅表软组织平滑肌肉瘤应该通过广泛的手术切除来治疗。建议浅表软组织多发平滑肌肉瘤患者应进一步检查,以排除腹膜后肿瘤的可能。最后,我们认为在诊断平滑肌肉瘤时,使用三色染色,如血红素-范吉森染色优于血红素-伊红染色。
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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