Malignant Hypertension and Paraganglioma in a 14-Year-Old Girl

Andıran, Nesibe; Köseoğlu,; Andıran, Fatih; Büyükpamukçu, Nebìl; Kutluk, Tezer; Büyükpamukçu, Münevver

doi:10.1080/088800199277623

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Cited by 4 publications

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“…6 Paraganglioma of the organ of Zuckerkandl has been described previously in multiple case reports. [7][8][9][10][11] Neuroblastomas arising from the organ of Zuckerkandl have also been described but are quite rare. 12 The majority of tumors of the organ of Zuckerkandl are benign, but a few are malignant.…”

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confidence: 99%

Laparoscopic Resection of a Paraganglioma of the Organ of Zuckerkandl in a Patient with a Carotid Body Tumor

Mithani

Marohn

Freischlag

et al. 2006

The American Surgeon™

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Paragangliomas of the organ of Zuckerkandl are rare tumors with only several case reports noted in the literature. Synchronous paraganglioma occur sporadically, and on occasion, in association with several genetic syndromes. Paraganglioma of the organ of Zuckerkandl with synchronous carotid body paraganglioma is described herein. Traditionally, surgical resection of abdominal paraganglioma involved an exploratory laparotomy. In this manuscript, we describe one of the first reported laparoscopic resections of this tumor and review the literature on multiple paragangliomas and their associated genetic syndromes.

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confidence: 99%