Literature DB >> 16027147

Hypokalemic rhabdomyolysis due to WDHA syndrome caused by VIP-producing composite pheochromocytoma: a case in neurofibromatosis type 1.

Masahiro Onozawa1, Takashi Fukuhara, Madoka Minoguchi, Mutsumi Takahata, Yasushi Yamamoto, Takayoshi Miyake, Koichi Kanagawa, Makoto Kanda, Isao Maekawa.   

Abstract

A 47-year-old woman with neurofibromatosis type 1 suffered from general muscle weakness and watery diarrhea. Laboratory findings showed elevated muscular enzymes, severe hypokalemia and excessive production of catecholamines and vasoactive intestinal polypeptide (VIP). A computed tomography scan showed a 10 cm left adrenal mass, in which [(131)I]-metaiodobenzylguanidine scintigraphy showed high uptake. After she underwent surgical removal of the tumor, all the symptoms and signs subsided. A histological study revealed that the mass consisted of pheochromocytoma and ganglioneuroma, respectively producing catecholamines and VIP. In immunohistochemical staining of neurofibromin, pheochromocytoma and ganglion cells showed positive staining, whereas the staining was negative for nerve bundles and Schwann cells. We concluded that the patient had hypokalemic rhabdomyolysis due to watery diarrhea, hypokalemia and achlorhydria (WDHA) syndrome, which was induced by a VIP-producing composite pheochromocytoma. Composite pheochromocytoma is a neuroendocrine tumor that is composed of pheochromocytoma and ganglioneuroma, both derived from the neural crest. Deficiency of neurofibromin in Schwann cells might have played an important role in the development and the growth of the composite pheochromocytoma in this patient.

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Year:  2005        PMID: 16027147     DOI: 10.1093/jjco/hyi139

Source DB:  PubMed          Journal:  Jpn J Clin Oncol        ISSN: 0368-2811            Impact factor:   3.019


  7 in total

1.  Composite Pheochromocytoma/Paraganglioma-Ganglioneuroma: A Clinicopathologic Study of Eight Cases with Analysis of Succinate Dehydrogenase.

Authors:  Sounak Gupta; Jun Zhang; Lori A Erickson
Journal:  Endocr Pathol       Date:  2017-09       Impact factor: 3.943

Review 2.  Watery diarrhea, hypokalemia and achlorhydria syndrome due to an adrenal pheochromocytoma.

Authors:  Shin-ichi Ikuta; Chiaki Yasui; Masahiro Kawanaka; Tsukasa Aihara; Hidenori Yoshie; Hidenori Yanagi; Masao Mitsunobu; Ayako Sugihara; Naoki Yamanaka
Journal:  World J Gastroenterol       Date:  2007-09-14       Impact factor: 5.742

3.  Case Report: Pheochromocytoma and Synchronous Neuroblastoma in a Family With Hereditary Pheochromocytoma Associated With a MAX Deleterious Variant.

Authors:  Diana Borges Duarte; Lia Ferreira; Ana P Santos; Cláudia Costa; Jorge Lima; Catarina Santos; Mariana Afonso; Manuel R Teixeira; Rui Carvalho; Maria Helena Cardoso
Journal:  Front Endocrinol (Lausanne)       Date:  2021-03-17       Impact factor: 5.555

Review 4.  Composite phaeochromocytomas-a systematic review of published literature.

Authors:  K Dhanasekar; V Visakan; F Tahir; S P Balasubramanian
Journal:  Langenbecks Arch Surg       Date:  2021-03-02       Impact factor: 2.895

5.  A rare case of watery diarrhea, hypokalemia and achlorhydria syndrome caused by pheochromocytoma.

Authors:  Jingjing Jiang; Li Zhang; Zhaodi Wu; Zhilong Ai; Yingyong Hou; Zhiqiang Lu; Xin Gao
Journal:  BMC Cancer       Date:  2014-07-31       Impact factor: 4.430

6.  Successful Treatment of Hypokalemic Rhabdomyolysis Caused by a Pancreatic VIPoma: A Case Report.

Authors:  Sergio Ramirez; Meghan Lytle; Enrique Togores; Jorge Parellada; Steve J Carlan; Mario Madruga; Rodrigo M Murillo-Alvarez
Journal:  Am J Case Rep       Date:  2019-11-22

Review 7.  A Novel Phenotype of Germline Pathogenic Variants in MAX: Concurrence of Pheochromocytoma and Ganglioneuroma in a Chinese Family and Literature Review.

Authors:  Xiaoyan Chang; Zelin Li; Xiaosen Ma; Yunying Cui; Shuchun Chen; Anli Tong
Journal:  Front Endocrinol (Lausanne)       Date:  2020-08-21       Impact factor: 5.555

  7 in total

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