[A case of costal haemangioma].

Abstract:

UNLABELLED:Costal primary tumors are rare and dominated by malignant tumors. Haemangioma of the bone represents only 1% of bone tumors. Costal localization accounts only for 1% of the cases and only about fifty cases have been reported in the literature. AIM:The authors aim to describe a rare costal tumor, its histological features and the main differential diagnoses. OBSERVATION:The authors describe the case of a 46-year-old woman who presented with chest pain. Radiological findings did not permit a malignant tumor to be ruled out and the treatment consisted of a resection of the posterior arch of the rib. Microscopic examination concluded that the patient had a costal haemangioma and the patient didn't present any recurrence after a six-year follow-up. CONCLUSION:The costal haemangioma is a very rare tumor with a debated etiology. Some radiological features are specific such as the "soap bubble" or "honeycomb" aspect. However, the basis for diagnosis remains microscopic examination. These tumors have a good prognosis and no cases of recurrence have been reported following complete resection.

journal_name

Rev Pneumol Clin

authors

Mlika M,Ayadi-Kaddour A,Racil H,Marghli A,Chabbou A,Kilani T,El Mezni F

doi

10.1016/j.pneumo.2010.11.005

subject

Has Abstract

pub_date

2011-12-01 00:00:00

pages

359-62

issue

6

eissn

0761-8417

issn

1776-2561

pii

S0761-8417(11)00019-8

journal_volume

67

pub_type

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