HMB-45 Negative Adrenal Angiomyolipoma With A Synchronous Adrenal Adenoma – An Unusual Association

Authors

  • Gayathri G Nair Amala Institute of Medical Sciences, Kerala, India
  • Sreeja Raju Amala Institute of Medical Sciences, Kerala, India
  • Joy Augustine Amala Institute of Medical Sciences, Kerala, India
  • Vijayalakshmi Nair Amala Institute of Medical Sciences, Kerala, India

DOI:

https://doi.org/10.21276/apalm.2826

Keywords:

Adenoma, Adrenal Angiomyolipoma, HMB-45 negative

Abstract

Background:

Angiomyolipoma (AML) is an uncommon mesenchymal tumour usually found in the kidney. The most common extrarenal site is usually the liver. We report a case of adrenal AML with a predominant vascular component co-existing with an adrenal adenoma.

Case report:

A fifty-year-old male presented with two months history of dysuria. Computed tomography showed a heterogeneous lesion involving the right adrenal gland abutting the right kidney and adjacent liver capsule.  Urine noradrenaline levels were elevated.  Adrenalectomy specimen showed an encapsulated mass measuring 8 x 5 x3.5 cm with a lobulated, grey to tan brown cut surface with areas of haemorrhage and tiny cystic spaces. Another yellowish nodule measuring 1.3 x 1.2 x 1 cm was also noted at one pole. Microscopy showed a neoplasm composed predominantly thick-walled vascular channels admixed with foci of smooth muscle bundles and adipocytes. Yellowish nodule showed features of adrenal adenoma.   HMB-45 was negative and CD34 positivity highlighted the thick and thin walled vessels.

Conclusion:

We present the very first case of HMB-45 negative adrenal AML with a predominant vascular component and a synchronous adrenal adenoma.

Author Biographies

Gayathri G Nair, Amala Institute of Medical Sciences, Kerala, India

Department of Pathology

Sreeja Raju, Amala Institute of Medical Sciences, Kerala, India

Department of Pathology

Joy Augustine, Amala Institute of Medical Sciences, Kerala, India

Department of Pathology

Vijayalakshmi Nair, Amala Institute of Medical Sciences, Kerala, India

Department of Pathology

References

1. Hussain T, Al-Hamali S. Pathophysiology and management aspects of adrenal angiomyolipomas. The Annals of The Royal College of Surgeons of England. 2012;94(4):224-226.
2. Ghimire O, Wenzheng L, Huaping L, Wenguang L, Yigang P, Jiale H. Angiomyolipoma of the Adrenal Gland: A Report of Two Cases and Review of the Literature. American Journal of Case Reports. 2017;18:989-994.
3. Sindhwani G,Jain A,Arora M,Patel V,Bhandari S,Ranga A.original article of renal angiomyolipomas: syndromic association, radiological diversity and management. International Journal of Scientific Research. 2017;6(9):174-177.
4. Lin C, Tsai C, Kau H, Yu W, Kao S, Liu C. HMB-45 negative angiomyolipoma of the orbit: a case report and review of the literature. BMC Ophthalmology. 2016;16(1).
5. Godara R, Vashist M, Singla S, Garg P, Sen J, Mathur S et al. Adrenal angiomyolipoma: A rare entity. Indian Journal of Urology. 2007;23(3):319.
6. Sharma A, Khullar R, Soni V, Baijal M, Chowbey P, Goswami A. Adrenal angiomyolipoma: A case report and review of literature. Journal of Minimal Access Surgery. 2014;10(4):213.
7. C. R. J, Menon D, Augustine J, Abdul Siyad A. Epithelioid Angiomyolipoma of Liver with an Inflammatory Component: A Case Report. Case Reports in Hepatology. 2013;2013:1-3.
8. Hu H, Xi X. Giant Adrenal Angiomyolipoma. The Journal of Clinical Endocrinology & Metabolism. 2012;97(11):3835-3836.
9. Aziz M, Tabrez M. A Giant Angiomyolipoma of the Adrenal Gland: A Rare Case Report with Review of Literature. New Indian Journal of Surgery. 2016;7(3):337-339.

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Published

01-09-2020

How to Cite

1.
Nair GG, Raju S, Augustine J, Nair V. HMB-45 Negative Adrenal Angiomyolipoma With A Synchronous Adrenal Adenoma – An Unusual Association. Ann of Pathol and Lab Med [Internet]. 2020 Sep. 1 [cited 2024 Dec. 5];7(8):C99-102. Available from: https://pacificejournals.com/journal/index.php/apalm/article/view/2826

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Section

Case Report