Yaseen Syed Besina, Mustafa Farhat, Rafiq Danish, Makhdoomi Rumana, Chanda Nassima
Department of Pathology, Sher-i-Kashmir Institute of Medical Sciences, Soura, Srinagar, Jammu and Kashmir, India.
J Cytol. 2015 Jan-Mar;32(1):56-8. doi: 10.4103/0970-9371.155240.
Synovial sarcomas are rare tumors accounting for approximately 5-10% of soft tissue sarcomas. They occur predominantly in the extremities, followed by head and neck. Primary pulmonary sarcomas are very rare and comprise only 0.5% of all primary lung malignancies. The diagnosis is established only after sarcomas like primary lung malignancies, and metastatic sarcomas have been excluded. For synovial sarcomas that arise at unusual locations, a definitive diagnosis is challenging and requires the use of ancillary diagnostic procedures such as immunohistochemistry (IHC) and molecular genetic techniques for confirmation of diagnosis. We report a case of 29-year-old male who had right lower lobe lung mass. He underwent right lower lobectomy. Intraoperative squash smears revealed spindle cell sarcoma. Subsequent histopathology and IHC confirmed the diagnosis as synovial sarcoma. We report this case on account of its rarity and to emphasize the utility of intraoperative squash smears in the diagnosis of such cases, which has been under-utilized in clinical practice.
滑膜肉瘤是罕见肿瘤,约占软组织肉瘤的5 - 10%。它们主要发生在四肢,其次是头颈部。原发性肺肉瘤非常罕见,仅占所有原发性肺恶性肿瘤的0.5%。只有在排除原发性肺恶性肿瘤和转移性肉瘤等肉瘤后才能确诊。对于发生在不寻常部位的滑膜肉瘤,明确诊断具有挑战性,需要使用免疫组织化学(IHC)和分子遗传学技术等辅助诊断程序来确诊。我们报告一例29岁男性,其右下叶有肺部肿块。他接受了右下叶切除术。术中压片涂片显示梭形细胞肉瘤。随后的组织病理学和免疫组织化学证实诊断为滑膜肉瘤。我们报告此病例是因其罕见性,并强调术中压片涂片在此类病例诊断中的实用性,而这在临床实践中未得到充分利用。