Rao B K, Kapur M M, Roy S
Dis Colon Rectum. 1980 Apr;23(3):184-90. doi: 10.1007/BF02587624.
Leiomyosarcoma of the colon, excluding that of the rectum, is extremely rare. We report a case of leiomyosarcoma of the ascending colon with a brief review of literature. The clinical manifestations in our case were typical: abdominal pain, diarrhea, anorexia, and a palpable tumor that was firm, smooth, and mobile inspite of its bulk. Toxic features, cachexia and weight loss were less prominent. Morphologically the tumor was of dumbbell type with intracolic and extracolic components. The microscopic picture, consisting of spindle-shaped smooth-muscle cells with pleomorphism and one to three mitotic figures per high-power field, was characteristic. In the absence of local spread, a hemicolectomy was considered curative, but our patient developed extensive metastasis in 25 months. The correlation between mitotic activity of the tumor and prognosis in our case was consistent with that reported in literature.
结肠平滑肌肉瘤(不包括直肠平滑肌肉瘤)极为罕见。我们报告一例升结肠平滑肌肉瘤病例,并对相关文献进行简要回顾。我们病例的临床表现具有典型性:腹痛、腹泻、厌食,可触及一个尽管体积较大但质地坚硬、表面光滑且可活动的肿瘤。中毒症状、恶病质和体重减轻不太明显。形态学上,肿瘤呈哑铃型,有结肠内和结肠外成分。显微镜下表现为梭形平滑肌细胞,具有多形性,每高倍视野有1至3个有丝分裂象,具有特征性。在无局部扩散的情况下,半结肠切除术被认为可治愈,但我们的患者在25个月后出现了广泛转移。我们病例中肿瘤的有丝分裂活性与预后之间的相关性与文献报道一致。