Sukpan Kornkanok, Khunamornpong Surapan, Suprasert Prapaporn, Siriaunkgul Sumalee
Department of Pathology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
J Med Assoc Thai. 2010 Apr;93(4):510-5.
The presence of osteoclast-like giant cells (OGC) has been reported as a rare and distinct feature in uterine leiomyosarcoma. To present knowledge, 11 cases have been described in the English literature. The authors report an additional example in a 35-year-old woman who presented with a pelvic mass. Pulmonary metastasis was detected by the preoperative CT scan. The hysterectomy specimen revealed a 11.5 cm intramural mass with hemorrhagic and necrotic center The histologic examination revealed pleomorphic sarcoma with OGC. The neoplastic cells were immunoreative for smooth muscle actin and desmin. Minor intermixing component of conventional leiomyosarcoma and leiomyoma were identified at the periphery of the malignant component. The patient died of disease after 16 months of diagnosis. To our knowledge, this is the youngest case of uterine leiomyosarcoma with OGC. Leiomyosarcoma with OGC has an aggressive clinical course. The tumor may occur in young patient and may arise from pre-existing leiomyoma.
破骨细胞样巨细胞(OGC)的存在已被报道为子宫平滑肌肉瘤中一种罕见且独特的特征。据目前所知,英文文献中已描述了11例。作者报告了另外1例,患者为一名35岁女性,表现为盆腔肿块。术前CT扫描检测到肺转移。子宫切除标本显示一个11.5 cm的壁间肿块,中心有出血和坏死。组织学检查显示为伴有OGC的多形性肉瘤。肿瘤细胞对平滑肌肌动蛋白和结蛋白呈免疫反应性。在恶性成分的周边发现了传统平滑肌肉瘤和平滑肌瘤的少量混合成分。患者在诊断后16个月死于疾病。据我们所知,这是子宫平滑肌肉瘤伴OGC最年轻的病例。伴有OGC的平滑肌肉瘤临床病程具有侵袭性。该肿瘤可能发生于年轻患者,且可能起源于既往存在的平滑肌瘤。