Sefiani S, Amarti A, Boulaadas M, Maher M, Saidi A
Hôpital Oto-Neuro-Ophtalmologique, Laboratoire d'Anatomie Pathologique, Rabat, Maroc.
Rev Laryngol Otol Rhinol (Bord). 2005;126(1):53-6.
Synovial sarcomas are soft tissue tumors that rarely occur in the head and neck The purpose of this report is to accrue data on this sarcoma at a rare site, and to highlight the histopathological differential diagnosis with other cervical tumors.
Two cases of cervico-facial tumors were reported in 26 and 27 year old women.
Histologically, these tumors were classified into monophasic and biphasic variants. Immunohistochemistry plays a major part in the differential diagnosis, enabling the demonstration of epithelial differentiation. Radical surgery was the mainstay of treatment with post-operative radiotherapy for residual disease in one case. Local recurrence was developed in the patient who had only surgical treatment.
Synovial sarcomas are a rare soft tissue malignancies and the head and neck region location accounts for 3-5% of them. The rarity of this tumor in the head and neck and its multitude of his histopathologic features are responsible for frequent initial misdiagnosis. Histologic, immunohistochemic and characteristic chromosomal translocation findings are necessary for diagnosis. The poor prognosis of this sarcoma justified a radical surgery with post-operative radiotherapy.
滑膜肉瘤是一种软组织肿瘤,很少发生于头颈部。本报告的目的是积累关于这种罕见部位肉瘤的数据,并突出其与其他颈部肿瘤的组织病理学鉴别诊断。
报告了2例发生于26岁和27岁女性的颈面部肿瘤。
组织学上,这些肿瘤分为单相型和双相型。免疫组织化学在鉴别诊断中起主要作用,可显示上皮分化。根治性手术是主要治疗方法,1例患者术后对残留病灶进行了放疗。仅接受手术治疗的患者出现了局部复发。
滑膜肉瘤是一种罕见的软组织恶性肿瘤,头颈部发病占3% - 5%。这种肿瘤在头颈部的罕见性及其众多的组织病理学特征导致了频繁的初始误诊。诊断需要组织学、免疫组织化学和特征性染色体易位结果。这种肉瘤的预后较差,因此采用根治性手术并术后放疗是合理的。