Primary glomangiosarcoma of the lung: A case report

Autor: Konstantinou Eleftheria, Kokkori Ioanna, Baliaka Aggeliki, Nikolaidou Anastasia, Asteriou Christos, Barbetakis Nikolaos, Kleontas Athanassios, Grigoriou Anna, Antzel Jacob
Jazyk: angličtina
Rok vydání: 2010
Předmět:
Zdroj: Journal of Cardiothoracic Surgery, Vol 5, Iss 1, p 76 (2010)
Druh dokumentu: article
ISSN: 1749-8090
DOI: 10.1186/1749-8090-5-76
Popis: Abstract Background Glomus tumor is an uncommon neoplasm derived from cells of the neuromyoarterial glomus or glomus body. Most glomus tumours occur in the dermis and subcutaneous tissues. A case of a primary pulmonary glomus tumour originating in the right upper lobe is presented. Case presentation A 74-yr-old male was admitted with siccus cough, dyspnea and right-sided chest pain. Computed tomography of the thorax revealed a 4 cm growth of the right upper lobe. Fiberoptic bronchoscopy demonstrated an endobronchial hypervascular mass causing obstruction of the apical segmental bronchus. Pathology report was consistent with pulmonary glomus tumor. The patient underwent a typical right upper lobectomy with mediastinal lymph node dissection. Twelve months later he is free of disease. Conclusion Occasionally glomus tumors can occur in extracutaneous sites such as the gastrointestinal tract, bone, genitourinary system and respiratory tract. Primary pulmonary glomus tumors are very rare (our case is the 19th one presented in the international literature) and are often confused with other solid neoplasms such as carcinoids, hemangiopericytomas and tumors belonging to the family of Ewing's sarcoma/primitive neuroectodermal tumours.
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