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10-year-old girl with life-threatening idiopathic systemic capillary leak syndrome: a case report
BACKGROUND: Idiopathic systemic capillary leak syndrome (ISCLS) is a rare disorder, characterized by episodic life-threatening hypotension, hypoalbuminemia, and hemoconcentration. CASE PRESENTATION: A 10-year-old girl presented with abdominal pain, vomiting, diarrhea, fever and developed generalized...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4229935/ https://www.ncbi.nlm.nih.gov/pubmed/24885961 http://dx.doi.org/10.1186/1471-2431-14-137 |
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author | Iwasa, Tadashi Ohashi, Hiroyuki Kihira, Kentaro Koike, Yuhki Otake, Kohei Inoue, Mikihiro Sawada, Hirofumi Toyoda, Hidemi Komada, Yoshihiro |
author_facet | Iwasa, Tadashi Ohashi, Hiroyuki Kihira, Kentaro Koike, Yuhki Otake, Kohei Inoue, Mikihiro Sawada, Hirofumi Toyoda, Hidemi Komada, Yoshihiro |
author_sort | Iwasa, Tadashi |
collection | PubMed |
description | BACKGROUND: Idiopathic systemic capillary leak syndrome (ISCLS) is a rare disorder, characterized by episodic life-threatening hypotension, hypoalbuminemia, and hemoconcentration. CASE PRESENTATION: A 10-year-old girl presented with abdominal pain, vomiting, diarrhea, fever and developed generalized edema a day after admission. Clinical and laboratory findings were consistent with ISCLS. She received aggressive fluid replacement, methylprednisolone pulse (30 mg/kg/day), high-dose intravenous immunoglobulin (IVIG, 2 g/kg/day) and plasma exchange in acute phase. She received fasciotomy of bilateral lower extremities as she developed complications of compartment syndrome. Since there were two episodes of ISCLS attacks, theophylline and terbutaline were initiated for prevention of attacks and then the remission is currently maintained. Because of high fatality rate in ISCLS, prompt diagnosis and intervention are very important. CONCLUSION: We describe here, a rare case of pediatric ISCLS. ISCLS should be considered as a differential diagnosis, when the patient presents with unexplained or sudden hypovolemic shock. Reports on pediatrics ISCLS are very few, and accumulation of similar case reports is needed. |
format | Online Article Text |
id | pubmed-4229935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42299352014-11-14 10-year-old girl with life-threatening idiopathic systemic capillary leak syndrome: a case report Iwasa, Tadashi Ohashi, Hiroyuki Kihira, Kentaro Koike, Yuhki Otake, Kohei Inoue, Mikihiro Sawada, Hirofumi Toyoda, Hidemi Komada, Yoshihiro BMC Pediatr Case Report BACKGROUND: Idiopathic systemic capillary leak syndrome (ISCLS) is a rare disorder, characterized by episodic life-threatening hypotension, hypoalbuminemia, and hemoconcentration. CASE PRESENTATION: A 10-year-old girl presented with abdominal pain, vomiting, diarrhea, fever and developed generalized edema a day after admission. Clinical and laboratory findings were consistent with ISCLS. She received aggressive fluid replacement, methylprednisolone pulse (30 mg/kg/day), high-dose intravenous immunoglobulin (IVIG, 2 g/kg/day) and plasma exchange in acute phase. She received fasciotomy of bilateral lower extremities as she developed complications of compartment syndrome. Since there were two episodes of ISCLS attacks, theophylline and terbutaline were initiated for prevention of attacks and then the remission is currently maintained. Because of high fatality rate in ISCLS, prompt diagnosis and intervention are very important. CONCLUSION: We describe here, a rare case of pediatric ISCLS. ISCLS should be considered as a differential diagnosis, when the patient presents with unexplained or sudden hypovolemic shock. Reports on pediatrics ISCLS are very few, and accumulation of similar case reports is needed. BioMed Central 2014-05-31 /pmc/articles/PMC4229935/ /pubmed/24885961 http://dx.doi.org/10.1186/1471-2431-14-137 Text en Copyright © 2014 Iwasa et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Case Report Iwasa, Tadashi Ohashi, Hiroyuki Kihira, Kentaro Koike, Yuhki Otake, Kohei Inoue, Mikihiro Sawada, Hirofumi Toyoda, Hidemi Komada, Yoshihiro 10-year-old girl with life-threatening idiopathic systemic capillary leak syndrome: a case report |
title | 10-year-old girl with life-threatening idiopathic systemic capillary leak syndrome: a case report |
title_full | 10-year-old girl with life-threatening idiopathic systemic capillary leak syndrome: a case report |
title_fullStr | 10-year-old girl with life-threatening idiopathic systemic capillary leak syndrome: a case report |
title_full_unstemmed | 10-year-old girl with life-threatening idiopathic systemic capillary leak syndrome: a case report |
title_short | 10-year-old girl with life-threatening idiopathic systemic capillary leak syndrome: a case report |
title_sort | 10-year-old girl with life-threatening idiopathic systemic capillary leak syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4229935/ https://www.ncbi.nlm.nih.gov/pubmed/24885961 http://dx.doi.org/10.1186/1471-2431-14-137 |
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