2019
551
04092018
29102018
Kelen Chistina A. Bezzerra ke_b@zipmail.com.br
Hospital São Francisco, Brazil
Djulienne Marly K. Reis
Hospital São Francisco, Brazil
Franciele Carla Prichoa
Hospital São Francisco, Brazil
ABSTRACT: The glomus tumor is a rare benign soft tissue tumor. We report a case of a 45-year-old male patient who presented with a painful mass in the abdominal wall. The patient underwent total tumor resection and the anatomical pathology diagnosis was of glomus tumor. The glomus tumor presents differential diagnosis of carcinoid tumor, hemangiopericytoma and vascular leiomyoma.
Key words: glomus tumorglomus tumor,abdominal wallabdominal wall,soft tissue tumorssoft tissue tumors.
RESUMEN: El tumor glómico es un tumor raro y benigno de tejidos blandos. Se presenta el caso de un paciente de 45 anos, con el hallazgo de un nódulo doloroso en la pared abdominal. Se realizó una resección completa de la lesión y el diagnóstico por anatomia patológica fue de tumor glómico. El diagnóstico diferencial del tumor glómico se plantea con tumor carcinoide, hemangiopericitoma y leiomioma vascular.
Palabras clave: tumor glómico, pared abdominal, tumor de tejidos blandos.
RESUMO: O tumor glômico é um tumor raro e benigno de tecidos moles. Relatamos o caso de um paciente do sexo masculino, 45 anos, que apresentava nódulo doloroso na parede abdominal. Foi realizada a ressecção total do tumor; o diagnóstico anatomopatológico foi de tumor glômico. Este apresenta diagnóstico diferencial, com tumor carcinoide, hemangiopericitoma e leiomioma vascular.
Unitermos: tumor glômico, parede abdominal, neoplasia de partes moles.
Case Report
Glomus tumor in the abdominal wall
Tumor glômico de parede abdominal
Kelen Chistina A. Bezzerra ke_b@zipmail.com.br
Received: 04 September 2018
Revised document received: 04 September 2018
Accepted: 29 October February 2018
The glomus tumor is a rare and benign soft tissue tumor. It is assumed that it originates from cells similar to the modified smooth muscle cells from the glomus body(1-3). Although it is more commonly found in the subungual region, it can also be found more rarely in places such as trachea, mediastinum, lungs, urinary bladder, skeletal muscle tissue and soft tissues(1,4). It occurs, in general, in middle-aged women(3,5).
A 45-year-old male patient presents painful nodular lesion on the abdominal wall. Total tumor resection was performed, and the material referred to pathological anatomy, whose gross-anatomy revealed a nodular lesion measuring 1.5 x 1.1 x 0.6 cm and microscopy, an encapsulated neoplasm consisting of round and small cells of eosinophilic cytoplasm and uniform nuclei, with no atypia, in solid block or arranged around blood vessels (Figures 1 and 2). Immunohistochemical analysis showed that the cells were positive for smooth muscle Actin (1A4), caldesmon (h-CALD) and type IV collagen (CIV 22). The final diagnosis was of glomus tumor.
Glomus tumors account for about 1.6% of all soft tissue neoplasms(1). They are believed to originate from cells similar to the modified smooth muscle cells of a neuromyoarterial glomus, or glomus body, which is a form of arteriovenous anastomosis that may be associated with thermoregulation(1,5). Surgical resection is usually curative, and recurrence of the lesion is rare(3).
CORRESPONDING AUTHOR Kelen Chistina Alves Bezzerra 0000-0001-7914-432X e-mail: ke_b@zipmail.com.br
