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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...

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Autores principales: Arunath, Visvalingam, Athapathu, Arjuna Salinda, Hoole, Thabitha Jebaseeli, Aruppala, Heshan, Rathnasri, Asanka, Ranawaka, Randula, Mettananda, Sachith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
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.
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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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