A rare coexistence of adrenal cavernous hemangioma with extramedullar hemopoietic tissue: a case report and brief review of the literature
- PMID: 19193247
- PMCID: PMC2647540
- DOI: 10.1186/1477-7819-7-13
A rare coexistence of adrenal cavernous hemangioma with extramedullar hemopoietic tissue: a case report and brief review of the literature
Abstract
Background: Cavernous hemangiomas of the adrenal gland are rare, benign, non-functioning neoplastic tumors. To our knowledge, 55 cases have been reported in the literature to date.
Case presentation: We report the first case of a large, non-functioning adrenal cavernous hemangioma that was incidentally found during the preoperative staging workup of a 75 year old woman with left breast adenocarcinoma. Imaging with US, CT scan and MRI showed a heterogeneous 8 cm mass with non-specific radiological features that was located on the left adrenal gland. The mass was surgically excised and pathology revealed an adrenal hemangioma with areas of extramedullar hemopoiesis.
Conclusion: Although adrenal hemangiomas are rare and their preoperative diagnosis is difficult, they should always be included in the differential diagnosis of adrenal neoplasms.
Figures
References
-
- Johnson CC, Jeppesen FB. Haemangioma of the adrenal. J Urol. 1955;74:573–577. - PubMed
-
- Heis HA, Bani-Hani KE, Bani-Hani BK. Adrenal cavernous haemangioma. Singapore Med J. 2008;49:e236–e237. - PubMed
-
- Makiyama K, Fukuoka H, Kawamoto K, Suwa Y. Surgical removal of adrenal haemangioma after five years of follow-up: a case report. Hinyokika Kiyo. 1998;44:579–581. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
