Literature DB >> 24825268

Pediatric and adolescent pheochromocytoma: clinical presentation and outcome of surgery.

Anjali Mishra1, Prateek Kumar Mehrotra, Gaurav Agarwal, Amit Agarwal, Saroj Kanta Mishra.   

Abstract

OBJECTIVES: To describe the clinical presentation and outcome of surgery in children with pheochromocytoma in a tertiary care hospital in India.
METHODS: Clinical records of 24 children who were operated between January 1990 and January 2011 were reviewed. The diagnosis of familial disease was established based on clinical examination and follow-up events.
RESULTS: Familial, bilateral, extra-adrenal and malignant pheochromocytoma were observed in 20.8%, 20.8%, 12.5% and 4.2% children, respectively. Median follow-up duration was 36 months. Persistent hypertension was noted in 12.5% patients and similar proportion died in follow-up.
CONCLUSIONS: In the absence of routine genetic screening, good history and long- term follow up are essential to rule out familial pheochromocytoma.

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Mesh:

Year:  2014        PMID: 24825268     DOI: 10.1007/s13312-014-0397-9

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN: 0019-6061            Impact factor:   1.411


  8 in total

1.  Genotype-Phenotype Correlation in Indian Patients with MEN2-Associated Pheochromocytoma and Comparison of Clinico-Pathological Attributes with Apparently Sporadic Adrenal Pheochromocytoma.

Authors:  Sendhil Rajan; Ghazala Zaidi; Gaurav Agarwal; Anjali Mishra; Amit Agarwal; Saroj Kanta Mishra; Eesh Bhatia
Journal:  World J Surg       Date:  2016-03       Impact factor: 3.352

2.  Clinical characteristics of adrenal tumors in children: a retrospective review of a 15-year single-center experience.

Authors:  Xiaokun Lin; Dazhou Wu; Congde Chen; Na Zheng
Journal:  Int Urol Nephrol       Date:  2016-12-17       Impact factor: 2.370

Review 3.  Pheochromocytoma and paraganglioma-an update on diagnosis, evaluation, and management.

Authors:  Amrish Jain; Rossana Baracco; Gaurav Kapur
Journal:  Pediatr Nephrol       Date:  2019-01-02       Impact factor: 3.714

4.  Minimally Invasive Surgery (MIS) in Children and Adolescents with Pheochromocytomas and Retroperitoneal Paragangliomas: Experiences in 42 Patients.

Authors:  Martin K Walz; Laura D Iova; Judith Deimel; Hartmut P H Neumann; Birke Bausch; Stefan Zschiedrich; Harald Groeben; Pier F Alesina
Journal:  World J Surg       Date:  2018-04       Impact factor: 3.352

Review 5.  Hypertension in Pheochromocytoma and Paraganglioma: Evaluation and Management in Pediatric Patients.

Authors:  Meredith L Seamon; Ikuyo Yamaguchi
Journal:  Curr Hypertens Rep       Date:  2021-05-27       Impact factor: 5.369

Review 6.  Characteristics of Pediatric Pheochromocytoma/paraganglioma.

Authors:  Vijaya Sarathi
Journal:  Indian J Endocrinol Metab       Date:  2017 May-Jun

7.  Pheochromocytoma and Paraganglioma in Children and Adolescents: Experience of the French Society of Pediatric Oncology (SFCE).

Authors:  Marie de Tersant; Lucile Généré; Claire Freyçon; Sophie Villebasse; Rachid Abbas; Anne Barlier; Damien Bodet; Nadège Corradini; Anne-Sophie Defachelles; Natacha Entz-Werle; Cyrielle Fouquet; Louise Galmiche; Virginie Gandemer; Brigitte Lacour; Ludovic Mansuy; Daniel Orbach; Claire Pluchart; Yves Réguerre; Charlotte Rigaud; Sabine Sarnacki; Nicolas Sirvent; Jean-Louis Stephan; Estelle Thebaud; Anne-Paule Gimenez-Roqueplo; Laurence Brugières
Journal:  J Endocr Soc       Date:  2020-04-03

8.  Clinical and genetic features of pediatric PCCs/PGLs patients: a single-center experience in China.

Authors:  Minghao Li; Cikui Wang; Peihua Liu; Lin Qi; Xiang Chen; Benyi Fan; Xiangyang Zhang; Bo Zhang; Qiao Xiao; Anze Yu; Longfei Liu
Journal:  Transl Androl Urol       Date:  2020-04
  8 in total

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