Metastatic neuroblastoma in a patient with ROHHAD: A new alert regarding the risk of aggressive malignancies in this rare condition-Reference-Cited by-同舟云学术

Metastatic neuroblastoma in a patient with ROHHAD: A new alert regarding the risk of aggressive malignancies in this rare condition

Published:2019-07-16 Issue: Volume: Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Calvo Charlotte¹^ORCID,Storey Caroline²,Morcrette Guillaume³,Akl Pia⁴,Fréneaux Paul⁵,Pierron Gaelle⁶,Trang Ha⁷,Aerts Isabelle¹^ORCID,Schleiermacher Gudrun¹,Philippe‐Chomette Pascale⁸,Carel Jean‐Claude²,Bourdeaut Franck¹

Affiliation:

1. SIREDO Pediatric Oncology CenterInstitut CurieParis Sciences Lettres University Paris France

2. Service d'endocrinologieAssistance Publique des Hôpitaux de ParisHôpital Robert Debré Paris France

3. Service de Pathologie and Université Diderot Paris 7/SPCAssistance Publique des Hôpitaux de ParisHôpital Universitaire Robert Debré Paris France

4. Medical Imaging DepartmentInstitut CurieParis Sciences Lettres University Paris France

5. Département de PathologieInstitut CurieParis Sciences Lettres University Paris France

6. Laboratory of Somatic GeneticsInstitut CurieParis Sciences Lettres University Paris France

7. Service de pneumologieAssistance Publique des Hôpitaux de ParisHôpital Robert Debré Paris France

8. Service de Chirurgie ViscéraleAssistance Publique des Hôpitaux de ParisHôpital Robert Debré Paris France

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.27906

Reference10 articles.

1. Germline gain-of-function mutations of ALK disrupt central nervous system development

2. ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome

3. Retinoblastoma and Neuroblastoma Predisposition and Surveillance

4. Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated WithPHOX2BNon-Polyalanine Repeat Expansion Mutations

5. Endocrine Manifestations of the Rapid-Onset Obesity with Hypoventilation, Hypothalamic, Autonomic Dysregulation, and Neural Tumor Syndrome in Childhood

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1. The Perfect Storm: A Case of Rapid-Onset Obesity With Hypoventilation, Hypothalamic, Autonomic Dysregulation, Neuroendocrine Tumor (ROHHADNET) With Heart Failure, Narcolepsy, and a Rare Location of a Pelvic Neuroendocrine Tumor;Cureus;2023-12-11

2. Whole genome sequencing in ROHHAD trios proved inconclusive: what’s beyond?;Frontiers in Genetics;2023-08-07

3. Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals;Journal of the Endocrine Society;2023-08-02

4. Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation (ROHHAD): a collaborative review of the current understanding;Clinical Autonomic Research;2023-05-10

5. ROHHAD syndrome – A still unrecognized cause of childhood obesity: report of three cases;Journal of Pediatric Endocrinology and Metabolism;2020-09-30