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Adrenal Cavernous Hemangioma: A Rarely Perceived Pathology-Case Illustration and Review of Literature

Overview
Journal Case Rep Pathol
Publisher Wiley
Specialty Pathology
Date 2020 Jan 18
PMID 31949968
Citations 10
Authors
Affiliations
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Abstract

Cavernous hemangiomas are endothelial tumors that rarely affect the adrenal glands. Most of these tumors remain silent and are incidentally found on abdominal imaging. Hardly ever, these tumors are endocrinologically functional. They may present as vague abdominal pain. Surgical resection remains the mainstay for large masses. In this paper, we are presenting a case of adrenal cavernous hemangioma in a 83-year-old male patient who initially presented for workup of vague abdominal and bilateral flank pain. A computed tomography scan of the abdomen showed an 8 cm right adrenal adenoma which was metabolically nonfunctional. The mass was completely resected through an open subcostal incision, with no encountered postoperative complications. A highlight of all published cases of adrenal hemangiomas since 1955 is also presented and reviewed.

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References
1.
Quint L, Glazer G, Francis I, Shapiro B, Chenevert T . Pheochromocytoma and paraganglioma: comparison of MR imaging with CT and I-131 MIBG scintigraphy. Radiology. 1987; 165(1):89-93. DOI: 10.1148/radiology.165.1.3628794. View

2.
Matsuda D, Iwamura M, Baba S . Cavernous hemangioma of the adrenal gland. Int J Urol. 2009; 16(4):424. DOI: 10.1111/j.1442-2042.2009.02260.x. View

3.
Aljabri K, Bokhari S, Alkeraithi M . Adrenal hemangioma in a 19-year-old female. Ann Saudi Med. 2011; 31(4):421-3. PMC: 3156522. DOI: 10.4103/0256-4947.76411. View

4.
Elfenbein D, Scarborough J, Speicher P, Scheri R . Comparison of laparoscopic versus open adrenalectomy: results from American College of Surgeons-National Surgery Quality Improvement Project. J Surg Res. 2013; 184(1):216-20. DOI: 10.1016/j.jss.2013.04.014. View

5.
Bhat H, Tiyadath B . Management of Adrenal Masses. Indian J Surg Oncol. 2017; 8(1):67-73. PMC: 5236029. DOI: 10.1007/s13193-016-0597-y. View