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Hermansky-Pudlak Syndrome: Case Report

Braz LS;
Jorge M;
Junior A;
Gomes JB;
Porto JM;
Fonseca DC;
Freitas MAV;
Oliveira KC;
Faria MR;
Pires RS;
Araujo RE;
Vieira RCGD;
Porto RM;
Santos CS;
Teixeira GW;
Santana HL;
Velasco JS

Lorenna da Silva Braz

Maurício Jorge

Andrade Junior

Julia Bergamini Gomes

Jully Miranda Porto

Daysa de Carvalho Fonseca

Maria Alice Vieira de Freitas

Katia Caetano de Oliveira

Marcelo Ribeiro Faria

Raiza Santos Pires

Rejane Estrela Araujo

Renata do Couto Gontijo de Deus Vieira

Renato Machado Porto

Claudio Silva Santos

Gabriella Waldraff Teixeira

Hernani Lopes Santana

Júlia Sanches de Velasco


Keywords

Hermansky-Pudlak syndrome
Pediatrics
Case report

Abstract

INTRODUCTION: Hermansky-Pudlak syndrome is a rare disease of autosomal recessive origin, with low incidences worldwide (1:1000000), except in Puerto Rico, whose incidence approaches 1:1800. It is composed of oculocutaneous albinism,  platelet dysfunction and,  in some cases,  there is pulmonary  fibrosis, insufficiency renal and colitis. The diagnosis is made by the clinic, ophthalmological and platelet count exams, as well as genetic testing to evaluate the prognosis.  The treatment is based on a  multidisciplinary approach to improve the quality of life since there is still no curative treatment.     CASE PRESENTATION: The patient, 2  years old,  consulted with a  pediatrician to evaluate abdominal pain, diarrhea with blood in the stool, and progressive weight loss for 2 months, also reporting a prolonged episode of epistaxis after local trauma.  On physical examination, oculocutaneous albinism and pulmonary auscultation with crackling rales at the base are noted. DISCUSSION: the most suitable optical resource was the Galileo 2.8x telescope. The treatment of granulomatous colitis is done through immunomodulatory therapy, performed in the treatment of Crohn's disease.  When the disease becomes refractory to treatment with medications, surgical interventions such as colectomy are performed. CONCLUSION: Because it is a rare syndrome and difficult to diagnose,  a better understanding of the pathogenesis of Hermansky syndrome is necessary.

 

DOI:https://doi.org/10.56238/devopinterscie-289


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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Copyright (c) 2023 Lorenna da Silva Braz, Maurício Jorge , Andrade Junior , Julia Bergamini Gomes, Jully Miranda Porto , Daysa de Carvalho Fonseca , Maria Alice Vieira de Freitas, Katia Caetano de Oliveira , Marcelo Ribeiro Faria , Raiza Santos Pires, Rejane Estrela Araujo, Renata do Couto Gontijo de Deus Vieira , Renato Machado Porto, Claudio Silva Santos , Gabriella Waldraff Teixeira , Hernani Lopes Santana

Author(s)

  • Lorenna da Silva Braz
  • Maurício Jorge
  • Andrade Junior
  • Julia Bergamini Gomes
  • Jully Miranda Porto
  • Daysa de Carvalho Fonseca
  • Maria Alice Vieira de Freitas
  • Katia Caetano de Oliveira
  • Marcelo Ribeiro Faria
  • Raiza Santos Pires
  • Rejane Estrela Araujo
  • Renata do Couto Gontijo de Deus Vieira
  • Renato Machado Porto
  • Claudio Silva Santos
  • Gabriella Waldraff Teixeira
  • Hernani Lopes Santana
  • Júlia Sanches de Velasco