[腹膜后肿瘤。腹膜后黏液样脂肪肉瘤。1例新病例报告]
[Retroperitoneal tumors. Retroperitoneal myxoid liposarcoma. Report of a new case].
作者信息
Azpiazu Arnaiz P, Muro Bidaurre I, De Frutos Gamero A, Castro Esnal E, Martín López A, Asensio Gallego J I, Ribera Garbayo J R
机构信息
Servicio de Cirugía General, Hospital de Guipuzcoa, San Sebastián, España.
出版信息
Arch Esp Urol. 2000 Mar;53(2):170-3.
OBJECTIVE
To describe an additional case of a large retroperitoneal liposarcoma.
METHODS/RESULTS: A case of a large retroperitoneal liposarcoma in a young male is presented. Treatment was by surgery. The clinical and pathological features, diagnosis, course and treatment of this lesion are discussed.
CONCLUSIONS
Retroperitoneal tumors constitute a heterogeneous group of uncommon neoplasms of unknown etiology. Liposarcoma is the most frequent lesion in this group. It is usually asymptomatic and is often identified by the presence of a large abdominal mass. It is considered to be a peculiar lesion because of its biological and morphological features and course.
目的
描述一例巨大腹膜后脂肪肉瘤的病例。
方法/结果：本文报告一名年轻男性的巨大腹膜后脂肪肉瘤病例。采用手术治疗。讨论了该病变的临床和病理特征、诊断、病程及治疗。
结论
腹膜后肿瘤是一组病因不明的罕见肿瘤，具有异质性。脂肪肉瘤是该组中最常见的病变。它通常无症状，常因腹部出现巨大肿块而被发现。由于其生物学、形态学特征及病程，它被认为是一种特殊的病变。
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