Literature DB >> 3922614

Malignant pheochromocytoma with ganglioneuroblastoma elements in a patient with von Recklinghausen's disease.

A Nakagawara, K Ikeda, M Tsuneyoshi, Y Daimaru, M Enjoji.   

Abstract

A 14-year-old girl with numerous café-au-lait spots in her skin was hospitalized because of fever, weight loss, and a mass of the right upper quadrant of the abdomen. Despite intensive chemotherapy, she died 6 months after admission. The autopsy revealed a right adrenal tumor with metastases to liver, lungs, vertebrae, and lymph nodes. Histologically the tumor was a pheochromocytoma with small foci of ganglioneuroblastoma. The catecholamine contents of the tumor were markedly elevated, as confirmed by the catecholamine fluorescence technique. Electron microscopically, the tumor cells contained intracytoplasmic membrane-bound chromaffin granules of varying sizes and shapes. This may be the first report of the concomitant occurrence of malignant catecholamine-secreting pheochromocytoma with ganglioneuroblastoma elements in a patient with von Recklinghausen's disease.

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Year:  1985        PMID: 3922614     DOI: 10.1002/1097-0142(19850615)55:12<2794::aid-cncr2820551213>3.0.co;2-l

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  8 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

2.  Sporadic type composite pheochromocytoma with neuroblastoma: clinicomorphologic, DNA content and ret gene analysis.

Authors:  F A Candanedo-González; I Alvarado-Cabrero; A Gamboa-Domínguez; A Cérbulo-Vázquez; R López-Romero; L Bornstein-Quevedo; M Salcedo-Vargas
Journal:  Endocr Pathol       Date:  2001       Impact factor: 3.943

3.  Unique association of non-functioning pheochromocytoma, ganglioneuroma, adrenal cortical adenoma, hepatic and vertebral hemangiomas in a patient with a new intronic variant in the VHL gene.

Authors:  G P Bernini; A Moretti; M Mannelli; T Ercolino; M Bardini; D Caramella; C Taurino; A Salvetti
Journal:  J Endocrinol Invest       Date:  2005-12       Impact factor: 4.256

4.  Composite Pheochromocytoma-Ganglioneuroma of the Adrenal Gland: An Uncommon Entity with Distinctive Clinicopathologic Features.

Authors:  King-Yin Lam; Chung-Yau Lo
Journal:  Endocr Pathol       Date:  1999       Impact factor: 3.943

5.  Composite adrenal medullary tumor: A rare cause of hypertension in a young male.

Authors:  Santosh Menon; Pravin Mahajan; Sangeeta B Desai
Journal:  Urol Ann       Date:  2011-01

6.  Concomitant compostite adrenal phoechromocytoma, multipte gastric stromal tumours and pseudohermaphrodism in a patient with von Recklinghausen's disease.

Authors:  Dean Lisewski; Simon Ryan; Ee Mun Lim; Felicity Frost; Hieu Nguyen
Journal:  Int Semin Surg Oncol       Date:  2006-04-26

7.  Expression of Extracellular Signal-regulated Kinase 5 and Ankyrin Repeat Domain 1 in Composite Pheochromocytoma and Ganglioneuroblastoma Detected Incidentally in the Adult Adrenal Gland.

Authors:  Shinta Suenaga; Osamu Ichiyanagi; Hiromi Ito; Sei Naito; Tomoyuki Kato; Akira Nagaoka; Tomoya Kato; Mitsunori Yamakawa; Yutaro Obara; Norihiko Tsuchiya
Journal:  Intern Med       Date:  2016-12-15       Impact factor: 1.271

Review 8.  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

  8 in total

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