Disseminated and late metastatic disease from nasal pit leiomyosarcoma after radical surgical resection. Case report of a singular presentation of a rare disease.

Clinical Sarcoma Research Pub Date : 2017-06-06 eCollection Date: 2017-01-01 DOI:10.1186/s13569-017-0078-2
Enrico Pinotti, Marta Sandini, Simone Famularo, Marta Jaconi, Fabrizio Romano, Luca Nespoli, Luca Gianotti
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引用次数: 2

Abstract

Background: Leiomyosarcoma of the head and neck is a rare cancer with high local aggressiveness. Radical surgery and adjuvant treatment offer the best chance for cure, nonetheless 5-years recurrence rate remains high. Despite international guidelines are available for soft tissue sarcomas, no recommendations are specifically endorsed for leiomyosarcoma of the head and neck, due to the rarity of its presentation and consequently scarcity of data on long-term outcome.

Case presentation: A 50-year old woman, operated 10 years before for leiomyosarcoma of the nasal pit and with negative 5-years follow-up, was admitted to our ward for impairment of the hepatic function. Total-body CT scan detected multiple localizations at lungs, kidneys, pancreas, bones, muscles, lymph nodes and thyroid. The pathologic report after lung biopsy confirmed the diagnosis of metastasis from leiomyosarcoma and the patients was scheduled for first line chemo-radiotherapy.

Conclusions: Despite adequate primary treatment, distant and disseminated metastatic disease may be not excluded in leiomyosarcoma of the head and neck.

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鼻窝平滑肌肉瘤根治性手术切除后的弥散性和晚期转移性疾病。一例罕见疾病的独特表现。
背景:头颈部平滑肌肉瘤是一种罕见的肿瘤,具有高度的局部侵袭性。根治性手术和辅助治疗提供了最好的治愈机会,但5年复发率仍然很高。尽管有针对软组织肉瘤的国际指南,但没有针对头颈部平滑肌肉瘤的特别推荐,因为其表现罕见,因此缺乏长期结果的数据。病例介绍:一名50岁女性,10年前因鼻窝平滑肌肉瘤手术,5年随访阴性,因肝功能损害住进我病房。全身CT扫描发现肺、肾、胰腺、骨骼、肌肉、淋巴结和甲状腺多发病灶。肺活检病理报告证实为平滑肌肉瘤转移,患者计划进行一线化疗。结论:尽管进行了适当的初步治疗,但头颈部平滑肌肉瘤可能不排除远处和播散性转移性疾病。
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期刊介绍: Clinical Sarcoma Research considers for publication articles related to research on sarcomas, including both soft tissue and bone. The journal publishes original articles and review articles on the diagnosis and treatment of sarcomas along with new insights in sarcoma research, which may be of immediate or future interest for diagnosis and treatment. The journal also considers negative results, especially those from studies on new agents, as it is vital for the medical community to learn whether new agents have been proven effective or ineffective within subtypes of sarcomas. The journal also aims to offer a forum for active discussion on topics of major interest for the sarcoma community, which may be related to both research results and methodological topics.
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