Cavernous hemangioma of the thymus: A case report and review of the literature

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Abstract

Rationale:

Cavernous hemangioma is a congenital venous malformation with the potential to develop in all tissues of the body. However, cavernous hemangioma of the thymus is extremely rare.

Patient concerns:

The present study describes the case of an asymptomatic, 30-year-old female who presented with a cavernous hemangioma in the thymus during a physical examination. Enhanced computed tomography of the chest revealed a 2.3 × 1.7 × 1.3 cm mass in the thymus.

Diagnoses:

Histopathological examination revealed that the tumor exhibited the typical histological findings of a cavernous hemangioma.

Interventions:

The patient underwent surgical resection due to the uncertain diagnosis and the possibility that the mass was a thymoma or teratoma.

Outcomes:

One-year post surgery, the patient was alive with no evidence of tumor recurrence.

Lessons:

Cavernous hemangioma of the thymus is a very rare disease. Complete surgical resection may be a critical therapeutic option.

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