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Severe Disfiguring Scalp and Facial Oedema due to Henoch–Schönlein Purpura in a Child
Henoch–Schönlein purpura is a small vessel vasculitis that usually presents with palpable purpura, arthritis, abdominal pain, and nephritis. Subcutaneous oedema of dependent areas is common; however, oedema in the scalp is extremely rare especially in children older than two years. Here, we report a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509540/ https://www.ncbi.nlm.nih.gov/pubmed/33005469 http://dx.doi.org/10.1155/2020/8823611 |
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author | Arunath, Visvalingam Athapathu, Arjuna Salinda Hoole, Thabitha Jebaseeli Aruppala, Heshan Rathnasri, Asanka Ranawaka, Randula Mettananda, Sachith |
author_facet | Arunath, Visvalingam Athapathu, Arjuna Salinda Hoole, Thabitha Jebaseeli Aruppala, Heshan Rathnasri, Asanka Ranawaka, Randula Mettananda, Sachith |
author_sort | Arunath, Visvalingam |
collection | PubMed |
description | Henoch–Schönlein purpura is a small vessel vasculitis that usually presents with palpable purpura, arthritis, abdominal pain, and nephritis. Subcutaneous oedema of dependent areas is common; however, oedema in the scalp is extremely rare especially in children older than two years. Here, we report a child with massive disfiguring scalp and facial oedema due to Henoch–Schönlein purpura. An eight-year-old boy presented with characteristic palpable purpuric rash and extensive disfiguring scalp and facial swelling for five days. He complained of blurred vision, vomiting, and severe headache on the day of admission. Examination revealed an ill child with extensive oedema of the face and scalp that was tender on palpation. His blood pressure was above the 99(th) percentile, and he had exaggerated deep tendon reflexes and extensor plantar responses. All biochemical investigations including renal function tests were normal. Noncontrast CT head showed normal brain, with marked soft tissue swelling of the scalp. Ultrasonography showed soft tissue oedema within and surrounding facial muscles without evidence of neck vessel compression. Urine analysis revealed microscopic haematuria on day 14 of the illness, and immunohistochemical staining of renal biopsy confirmed Henoch–Schönlein purpura nephritis. In conclusion, this case report presents a child with severe, disfiguring scalp and facial oedema due to Henoch–Schönlein purpura. It highlights that severe subcutaneous oedema of Henoch–Schönlein purpura can involve any part of the body not limiting to dependent areas. |
format | Online Article Text |
id | pubmed-7509540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-75095402020-09-30 Severe Disfiguring Scalp and Facial Oedema due to Henoch–Schönlein Purpura in a Child Arunath, Visvalingam Athapathu, Arjuna Salinda Hoole, Thabitha Jebaseeli Aruppala, Heshan Rathnasri, Asanka Ranawaka, Randula Mettananda, Sachith Case Rep Pediatr Case Report Henoch–Schönlein purpura is a small vessel vasculitis that usually presents with palpable purpura, arthritis, abdominal pain, and nephritis. Subcutaneous oedema of dependent areas is common; however, oedema in the scalp is extremely rare especially in children older than two years. Here, we report a child with massive disfiguring scalp and facial oedema due to Henoch–Schönlein purpura. An eight-year-old boy presented with characteristic palpable purpuric rash and extensive disfiguring scalp and facial swelling for five days. He complained of blurred vision, vomiting, and severe headache on the day of admission. Examination revealed an ill child with extensive oedema of the face and scalp that was tender on palpation. His blood pressure was above the 99(th) percentile, and he had exaggerated deep tendon reflexes and extensor plantar responses. All biochemical investigations including renal function tests were normal. Noncontrast CT head showed normal brain, with marked soft tissue swelling of the scalp. Ultrasonography showed soft tissue oedema within and surrounding facial muscles without evidence of neck vessel compression. Urine analysis revealed microscopic haematuria on day 14 of the illness, and immunohistochemical staining of renal biopsy confirmed Henoch–Schönlein purpura nephritis. In conclusion, this case report presents a child with severe, disfiguring scalp and facial oedema due to Henoch–Schönlein purpura. It highlights that severe subcutaneous oedema of Henoch–Schönlein purpura can involve any part of the body not limiting to dependent areas. Hindawi 2020-09-14 /pmc/articles/PMC7509540/ /pubmed/33005469 http://dx.doi.org/10.1155/2020/8823611 Text en Copyright © 2020 Visvalingam Arunath et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Arunath, Visvalingam Athapathu, Arjuna Salinda Hoole, Thabitha Jebaseeli Aruppala, Heshan Rathnasri, Asanka Ranawaka, Randula Mettananda, Sachith Severe Disfiguring Scalp and Facial Oedema due to Henoch–Schönlein Purpura in a Child |
title | Severe Disfiguring Scalp and Facial Oedema due to Henoch–Schönlein Purpura in a Child |
title_full | Severe Disfiguring Scalp and Facial Oedema due to Henoch–Schönlein Purpura in a Child |
title_fullStr | Severe Disfiguring Scalp and Facial Oedema due to Henoch–Schönlein Purpura in a Child |
title_full_unstemmed | Severe Disfiguring Scalp and Facial Oedema due to Henoch–Schönlein Purpura in a Child |
title_short | Severe Disfiguring Scalp and Facial Oedema due to Henoch–Schönlein Purpura in a Child |
title_sort | severe disfiguring scalp and facial oedema due to henoch–schönlein purpura in a child |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509540/ https://www.ncbi.nlm.nih.gov/pubmed/33005469 http://dx.doi.org/10.1155/2020/8823611 |
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