Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2023 Jul-Aug;28(4):328-331.
doi: 10.4103/jiaps.jiaps_11_23. Epub 2023 Jul 11.

Bilateral Synchronous Robotic-Assisted Adrenalectomies in a Patient of Bilateral Pheochromocytoma and Von Hippel-Lindau Disease - A Rewarding Approach

Affiliations
Case Reports

Bilateral Synchronous Robotic-Assisted Adrenalectomies in a Patient of Bilateral Pheochromocytoma and Von Hippel-Lindau Disease - A Rewarding Approach

Ashitosh D Pokharkar et al. J Indian Assoc Pediatr Surg. 2023 Jul-Aug.

Abstract

Hypertensive crisis is rare in children. Among the rarest causes leading to this acute crisis, is bilateral adrenal tumour as a part of a syndrome, Von Hippel Lindau syndrome. The treatment is based on the excision of the adrenal tumour followed by long term surviellence. The authors present a case where conventional imaging with ultrasound and contrast enhanced CT scan demonstrated a right side adrenal tumour with raised catecholamines. The small left side tumour got missed on conventional imaging and got picked up on DOTA scan. The persistence of hypertension in post operative period can be related to such hidden functioning tumours. In view of the size of tumour & raised dopamine associated with high incidence of malignancy, robotic surgery was used for bilateral adrenal tumour excision which confirmed the diagnosis of Pheochromocytoma (PCC).

Keywords: 68Ga-DOTA positron emission tomography/computed tomography scan; Von Hippel–Lindau disease; pheochromocytoma; robotic adrenalectomy.

PubMed Disclaimer

Conflict of interest statement

There are no conflicts of interest.

Figures

Figure 1
Figure 1
6 cm × 4 cm mass of right adrenals
Figure 2
Figure 2
Left adrenal mass in yellow pointer
Figure 3
Figure 3
Schematic representation of abdominal port positions

Similar articles

Cited by

References

    1. Trompeter RS, Smith RL, Hoare RD, Neville BG, Chantler C. Neurological complications of arterial hypertension. Arch Dis Child. 1982;57:913–7. - PMC - PubMed
    1. Uhari M, Saukkonen AL, Koskimies O. Central nervous system involvement in severe arterial hypertension of childhood. Eur J Pediatr. 1979;132:141–6. - PubMed
    1. Januszewicz P, Wieteska-Klimczak A, Wyszyńska T. Pheochromocytoma in children: Difficulties in diagnosis and localization. Clin Exp Hypertens A. 1990;12:571–9. - PubMed
    1. Lonser RR, Glenn GM, Walther M, Chew EY, Libutti SK, Linehan WM, et al. von Hippel-Lindau disease. Lancet. 2003;361:2059–67. - PubMed
    1. Baghai M, Thompson GB, Young WF, Jr, Grant CS, Michels VV, van Heerden JA. Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: A role for laparoscopic and cortical-sparing surgery. Arch Surg. 2002;137:682–8. - PubMed

Publication types