Cargando…

Self-Healing Juvenile Cutaneous Mucinosis: A Case Report in the Middle East

Patient: Male, 12 Final Diagnosis: Self-healing juvenile cutaneous mucinosis Symptoms: Facial edema • nodular skin lesion Medication: — Clinical Procedure: None Specialty: Pediatrics and Neonatology OBJECTIVE: Rare disease BACKGROUND: Self-healing juvenile cutaneous mucinosis (SHJCM) is a rarely dia...

Descripción completa

Detalles Bibliográficos
Autores principales: Geagea, Caroline, Youssef, Nour, Wakim, Gerard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345112/
https://www.ncbi.nlm.nih.gov/pubmed/30647403
http://dx.doi.org/10.12659/AJCR.910047
_version_ 1783389531857223680
author Geagea, Caroline
Youssef, Nour
Wakim, Gerard
author_facet Geagea, Caroline
Youssef, Nour
Wakim, Gerard
author_sort Geagea, Caroline
collection PubMed
description Patient: Male, 12 Final Diagnosis: Self-healing juvenile cutaneous mucinosis Symptoms: Facial edema • nodular skin lesion Medication: — Clinical Procedure: None Specialty: Pediatrics and Neonatology OBJECTIVE: Rare disease BACKGROUND: Self-healing juvenile cutaneous mucinosis (SHJCM) is a rarely diagnosed disease worldwide, with less than 20 reported cases in the literature. It is characterized by a rather benign course in juvenile patients with nodular and mucinous skin eruption and edema. CASE REPORT: A 12-year-old male patient previously healthy presented to the pediatrics clinic with a 1-week history of bilateral palmer pruritus and plantar tenderness upon walking, preceded by eruption of erythematous patch on his neck. The disease course evolved to include facial edema, erythema, nodular skin eruptions with a completely negative initial workup. The patient was labelled as a juvenile idiopathic arthritis patient and doomed to be a candidate for corticosteroid therapy. Upon further workup, a skin biopsy was taken and SHJCM was diagnosed. Complete resolution of symptoms was witnessed on symptomatic treatment after 5 months of diagnosis. CONCLUSIONS: To our knowledge, this is the second case of SHJCM reported in the Middle East and the first to be reported in Lebanon. It is also the first case reported to have the longest follow-up period; 10 years of follow-up with no new findings or relapse. SHJCM is a rare disease whereby awareness of its features and presentation may help in diagnosing it and preventing unnecessary testing and aggressive treatment for a rather benign disease.
format Online
Article
Text
id pubmed-6345112
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher International Scientific Literature, Inc.
record_format MEDLINE/PubMed
spelling pubmed-63451122019-02-11 Self-Healing Juvenile Cutaneous Mucinosis: A Case Report in the Middle East Geagea, Caroline Youssef, Nour Wakim, Gerard Am J Case Rep Articles Patient: Male, 12 Final Diagnosis: Self-healing juvenile cutaneous mucinosis Symptoms: Facial edema • nodular skin lesion Medication: — Clinical Procedure: None Specialty: Pediatrics and Neonatology OBJECTIVE: Rare disease BACKGROUND: Self-healing juvenile cutaneous mucinosis (SHJCM) is a rarely diagnosed disease worldwide, with less than 20 reported cases in the literature. It is characterized by a rather benign course in juvenile patients with nodular and mucinous skin eruption and edema. CASE REPORT: A 12-year-old male patient previously healthy presented to the pediatrics clinic with a 1-week history of bilateral palmer pruritus and plantar tenderness upon walking, preceded by eruption of erythematous patch on his neck. The disease course evolved to include facial edema, erythema, nodular skin eruptions with a completely negative initial workup. The patient was labelled as a juvenile idiopathic arthritis patient and doomed to be a candidate for corticosteroid therapy. Upon further workup, a skin biopsy was taken and SHJCM was diagnosed. Complete resolution of symptoms was witnessed on symptomatic treatment after 5 months of diagnosis. CONCLUSIONS: To our knowledge, this is the second case of SHJCM reported in the Middle East and the first to be reported in Lebanon. It is also the first case reported to have the longest follow-up period; 10 years of follow-up with no new findings or relapse. SHJCM is a rare disease whereby awareness of its features and presentation may help in diagnosing it and preventing unnecessary testing and aggressive treatment for a rather benign disease. International Scientific Literature, Inc. 2019-01-16 /pmc/articles/PMC6345112/ /pubmed/30647403 http://dx.doi.org/10.12659/AJCR.910047 Text en © Am J Case Rep, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Geagea, Caroline
Youssef, Nour
Wakim, Gerard
Self-Healing Juvenile Cutaneous Mucinosis: A Case Report in the Middle East
title Self-Healing Juvenile Cutaneous Mucinosis: A Case Report in the Middle East
title_full Self-Healing Juvenile Cutaneous Mucinosis: A Case Report in the Middle East
title_fullStr Self-Healing Juvenile Cutaneous Mucinosis: A Case Report in the Middle East
title_full_unstemmed Self-Healing Juvenile Cutaneous Mucinosis: A Case Report in the Middle East
title_short Self-Healing Juvenile Cutaneous Mucinosis: A Case Report in the Middle East
title_sort self-healing juvenile cutaneous mucinosis: a case report in the middle east
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345112/
https://www.ncbi.nlm.nih.gov/pubmed/30647403
http://dx.doi.org/10.12659/AJCR.910047
work_keys_str_mv AT geageacaroline selfhealingjuvenilecutaneousmucinosisacasereportinthemiddleeast
AT youssefnour selfhealingjuvenilecutaneousmucinosisacasereportinthemiddleeast
AT wakimgerard selfhealingjuvenilecutaneousmucinosisacasereportinthemiddleeast