PDF herunterladen
CC BY-NC-ND 4.0 · Journal of Health and Allied Sciences NU 2022; 12(01): 87-89
DOI: 10.1055/s-0041-1730745
Case Report

Adrenal Hemangioma: A Common Tumor at Uncommon Site

Ritu Asnani
1   Department of Pathology, K.S. Hegde Medical Academy, Nitte (deemed to be University), Mangalore, Karnataka, India
,
Kishan Prasad Hosapatna Laxminarayana
1   Department of Pathology, K.S. Hegde Medical Academy, Nitte (deemed to be University), Mangalore, Karnataka, India
,
Sajitha Kaliyat
1   Department of Pathology, K.S. Hegde Medical Academy, Nitte (deemed to be University), Mangalore, Karnataka, India
,
Kalale R. Bhagvan
2   Department of General Surgery, K.S. Hegde Medical Academy, Nitte (deemed to be University), Mangalore, Karnataka, India
,
Praveen Kumar R. Bhat
2   Department of General Surgery, K.S. Hegde Medical Academy, Nitte (deemed to be University), Mangalore, Karnataka, India
,
Shreya Goel
1   Department of Pathology, K.S. Hegde Medical Academy, Nitte (deemed to be University), Mangalore, Karnataka, India
› Institutsangaben
› Weitere Informationen
   Lizenzen und Reprints

Abstract

Adrenal hemangiomas are rare vascular tumors. These are benign, mostly nonfunctioning and asymptomatic. Cavernous adrenal hemangiomas are more common in the elderly, with female preponderance. A computed tomography (CT) scan can diagnose their benign nature. Most cases are managed surgically, and laparoscopy is the most common approach followed nowadays.

A young female presented with nausea, pain, and a vague mass palpable in the right abdomen. With CT findings favoring benign lesion or nonfunctioning adenoma but symptomatic, the patient had to undergo diagnostic laparoscopy and adrenalectomy. Adrenal hemangiomas are rare lesions. Moreover, involving a young female further makes their diagnosis difficult. Hence, they must be kept as one of the differential diagnosis in evaluation of adrenal mass in young females.

Keywords

cavernous hemangiomas - benign tumors - dilated vascular channels


Publikationsverlauf

Artikel online veröffentlicht:
04. Juni 2021

© 2021. Nitte (Deemed to be University). Nitte University. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India

 

  • References

  • 1 Mitchell RN. Blood vessels. In: Robbins and Cotran Pathologic Basis of Disease. 9th edition 2015: 483-521
  • 2 Degheili JA, Abou Heidar NF, El-Moussawi M, Tawil A, Nasr RW. Adrenal cavernous hemangioma: a rarely perceived pathology-case illustration and review of the literature. Case Rep Pathol 2019; 2019: 8463890 DOI: 10.1155/2019/8463890.
    CrossrefPubMedGoogle Scholar
  • 3 Feo CV, De Troia A, Pedriali M. et al Adrenal cavernous hemangioma: a case report. BMC Surg 2018; 18 (01) 103
    CrossrefPubMedGoogle Scholar
  • 4 Zemni I, Haddad S, Hlali A, Manai MH, Essoussi M. Adrenal gland hemangioma: a rare case of the incidentaloma: case report. Int J Surg Case Rep 2017; 41: 417-422
    CrossrefPubMedGoogle Scholar
  • 5 Pang C, Wu P, Zhu G. A rare cavernous hemangioma of the adrenal gland. Urol Case Rep 2015; 3 (04) 120-122
    CrossrefPubMedGoogle Scholar
  • 6 Oishi M, Ueda S, Honjo S, Koshiyama H, Yuba Y, Takabayashi A. Adrenal cavernous hemangioma with subclinical Cushing’s syndrome: report of a case. Surg Today 2012; 42 (10) 973-977
    CrossrefPubMedGoogle Scholar
  • 7 Ng AC, Loh HL, Shum CF, Yip SK. A case of adrenal cavernous hemangioma presenting with progressive enlargement and apparent hormonal hypersecretion. Endocr Pract 2008; 14 (01) 104-108
    CrossrefPubMedGoogle Scholar
  • 8 Paluszkiewicz P, Ambroziak I, Hołyńska-Dąbrowska K, Siezieniewska-Skowrońska Z, Paluszkiewicz A. Spontaneous rupture of adrenal haemangioma mimicking abdominal aortic aneurysm rupture. Arch Med Sci 2010; 6 (01) 122-125
    CrossrefPubMedGoogle Scholar
  • 9 Ishigami K, Stolpen AH, Sato Y, Dahmoush L, Winfield HN, Fajardo LL. Adrenal adenoma with organizing hematoma: diagnostic dilemma at MRI. Magn Reson Imaging 2004; 22 (08) 1157-1159
    CrossrefPubMedGoogle Scholar
  • 10 Elfenbein DM, Scarborough JE, Speicher PJ, Scheri RP. Comparison of laparoscopic versus open adrenalectomy: results from American College of Surgeons-National Surgery Quality Improvement Project. J Surg Res 2013; 184 (01) 216-220
    CrossrefPubMedGoogle Scholar