Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

Cecilia Lazea1 Department of Pediatrics I, Emergency Clinic Hospital for Children, “Iuliu Hatieganu” University of Medicine and Pharmacy, [email protected]Correspondence[email protected]

Carmen Asavoaie2 Department of Imaging and Radiology, Emergency Clinic Hospital for Children

Camelia Al-Khzouz3 Medical Genetics Department, Emergency Clinic Hospital for Children, University of Medicine and Pharmacy, Cluj-Napoca, Romania

Lenuta Popa1 Department of Pediatrics I, Emergency Clinic Hospital for Children, “Iuliu Hatieganu” University of Medicine and Pharmacy, [email protected]

Pages 1547-1552 | Published online: 31 Aug 2018

Cite this article
CrossMark

Full Article
Figures & data
References
Citations
Metrics
Licensing
Reprints & Permissions
View PDF PDF

References

ReynoldsRMBrowningGGNawrozICampbellIWvon Reckling-hausen’s neurofibromatosis: neurofibromatosis type 1Lancet200336193681552155412737880
PubMed Web of Science ®Google Scholar
HamiltonSJFriedmanJMInsights into the pathogenesis of neurofibromatosis 1 vasculopathyClin Genet200058534134411140831
PubMed Web of Science ®Google Scholar
ShahUGiubellinoAPacakKPheochromocytoma: implications in tumorigenesis and the actual managementMinerva Endocrinol201237214115622691888
PubMed Web of Science ®Google Scholar
FernerREHusonSMThomasNGuidelines for the diagnosis and management of individuals with neurofibromatosis 1J Med Genet2007442818
Web of Science ®Google Scholar
DubovTToledano-AlhadefHCherninGConstantiniSCleperRBen-ShacharSHigh prevalence of elevated blood pressure among children with neurofibromatosis type 1Pediatr Nephrol201631113113626314566
PubMed Web of Science ®Google Scholar
FlynnJTKaelberDCBaker-SmithCMClinical practice guideline for screening and management of high blood pressure in children and adolescentsPediatrics20171403e2017190428827377
PubMed Web of Science ®Google Scholar
LendersJWDuhQYEisenhoferGPheochromocytoma and paraganglioma: an Endocrine Society clinical practice guidelineJ Clin Endocrinol Metab20149961915194224893135
PubMed Web of Science ®Google Scholar
WaltherMMHerringJEnquistEKeiserHRLinehanWMvon Recklinghausen’s disease and pheochromocytomasJ Urol199916251582158610524872
PubMed Web of Science ®Google Scholar
KépénékianLMognettiTLifanteJCInterest of systematic screening of pheochromocytoma in patients with neurofibromatosis type 1Eur J Endocrinol2016175433534427450695
PubMed Web of Science ®Google Scholar
CostaMHOrtiga-CarvalhoTVolanteADValsmanMPheochromocytomas and paragangliomas: clinical and genetic approachesFront Endocrinol20156126
PubMed Web of Science ®Google Scholar
AhmedRDarratYHamoudehEElhamdaniMOYaqubAAcute cardiomyopathy and multiorgan failure in a patient with pheochromocytoma and neurofibromatosis type 1J Pak Med Assoc201464221421624640818
PubMed Web of Science ®Google Scholar
EisenhoferGTimmersHJLendersJWAge at diagnosis of pheochromocytoma differs according to catecholamine phenotype and tumor locationJ Clin Endocrinol Metab201196237538421147885
PubMed Web of Science ®Google Scholar
CecchinDLumachiFMarzolaMCA meta-iodobenzylguanidine scintigraphic scoring system increases accuracy in the diagnostic management of pheochromocytomaEndocr Relat Cancer200613252553316728579
PubMed Web of Science ®Google Scholar
EisenhoferGLendersJWGoldsteinDSPheochromocytoma catecholamine phenotypes and prediction of tumor size and location by use of plasma free metanephrinesClin Chem200551473574415718487
PubMed Web of Science ®Google Scholar
LloydRVAdrenal cortical tumors, pheochromocytomas and paragangliomasMod Pathol201124Suppl 2S58S6521455202
PubMed Web of Science ®Google Scholar
OderichGSSullivanTMBowerTCVascular abnormalities in patients with neurofibromatosis syndrome type I: clinical spectrum, management, and resultsJ Vasc Surg200746347548417681709
PubMed Web of Science ®Google Scholar
RummanRKNickelCMatsuda-AbediniMDisease beyond the arch: a systematic review of middle aortic syndrome in childhoodAm J Hypertens201528783384625631383
PubMed Web of Science ®Google Scholar
PorrasDSteinDRFergusonMAMidaortic syndrome: 30 years of experience with medical, endovascular and surgical managementPediatr Nephrol201328102023203323775038
PubMed Web of Science ®Google Scholar
BarralXde LatourBVolaMLavocatMPFichtnerCFavreJPSurgery of the abdominal aorta and its branches in children: late follow-upJ Vasc Surg20064361138114416765229
PubMed Web of Science ®Google Scholar

Share icon
Back to Top

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.

People also read
Recommended articles
Cited by

To cite this article:

Reference style: APA Chicago Harvard

Citation copied to clipboard

Reference styles above use APA (6th edition), Chicago (16th edition) & Harvard (10th edition)

Download citation

Download a citation file in RIS format that can be imported by citation management software including EndNote, ProCite, RefWorks and Reference Manager.

Choose format: RIS BibTex RefWorks Direct Export

Choose options: Citation Citation & abstract Citation & references

Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

References

Information for

Open access

Opportunities

Help and information

Your download is now in progress and you may close this window

Login or register to access this feature

Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

References

Related research

To cite this article:

Download citation

Information for

Open access

Opportunities

Help and information

Keep up to date