Acute Soft Head Syndrome as the Initial Presentation of Sickle Cell Disease in an Adolescent in Rural Western Uganda: Case Report

Sickle haemoglobin (HbS) is the most common abnormal haemoglobin mutation worldwide. In Uganda, according to the Uganda Sickle Surveillance Study (US3), the overall prevalence of sickle cell trait and disease is 13.3% and 0.7%, respectively. SCD presents with numerous complications. Acute Soft Head...

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Main Authors: Abukar Ali Ahmed, Dalton Kambale Munyambalu, Awil Abdulkadir Abdi, Elias Joseph Xwatsal, Hanan Asad Hassan, Ibrahim Ahmed Nur, Abdikani Ali Hassan, Venance Emmanuel Mswelo
Format: Article
Language:English
Published: QAASPA Publisher 2024-12-01
Series:BioMed Target Journal
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Online Access:https://qaaspa.com/index.php/bmtj/article/view/28
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author Abukar Ali Ahmed
Dalton Kambale Munyambalu
Awil Abdulkadir Abdi
Elias Joseph Xwatsal
Hanan Asad Hassan
Ibrahim Ahmed Nur
Abdikani Ali Hassan
Venance Emmanuel Mswelo
author_facet Abukar Ali Ahmed
Dalton Kambale Munyambalu
Awil Abdulkadir Abdi
Elias Joseph Xwatsal
Hanan Asad Hassan
Ibrahim Ahmed Nur
Abdikani Ali Hassan
Venance Emmanuel Mswelo
author_sort Abukar Ali Ahmed
collection DOAJ
description Sickle haemoglobin (HbS) is the most common abnormal haemoglobin mutation worldwide. In Uganda, according to the Uganda Sickle Surveillance Study (US3), the overall prevalence of sickle cell trait and disease is 13.3% and 0.7%, respectively. SCD presents with numerous complications. Acute Soft Head Syndrome (ASHS) or sickle cell cephalohematoma is among the rare complications of SCD. We report a 14-year-old adolescent male, a resident of rural Western Uganda, who presented with a history of non-traumatic painless scalp swelling for a week and multiple joints pain for 5 days. He had a similar swelling in the previous six months, which subsided after blood transfusion given at a nearby health facility. There was a history of on-and-off fever, easy fatiguability, and generalized body weakness. Complete blood counts revealed anemia, Haemoglobin Electrophoresis confirmed Sickle Cell Anemia. Head Computed Tomography concluded a subgaleal fluid collection. The diagnosis of acute soft head syndrome was established in a newly diagnosed SCD patient. This case highlights a rare diagnosis of acute soft head syndrome as well as a late diagnosis of SCD in adolescent in rural settings. In such settings, the pre-existing poor socio-economic background coupled with atypical presentation constitute a major impediment for timely diagnosis.
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spelling doaj-art-b19bae47383e40869f1e89bc1a21e0e02025-01-10T21:54:26ZengQAASPA PublisherBioMed Target Journal2960-14282024-12-0122717410.59786/bmtj.22728Acute Soft Head Syndrome as the Initial Presentation of Sickle Cell Disease in an Adolescent in Rural Western Uganda: Case ReportAbukar Ali Ahmed0https://orcid.org/0009-0005-8710-8421Dalton Kambale Munyambalu1https://orcid.org/0000-0002-7055-6552Awil Abdulkadir Abdi2https://orcid.org/0009-0001-1983-3470Elias Joseph Xwatsal3https://orcid.org/0009-0008-7379-0441Hanan Asad Hassan4https://orcid.org/0009-0005-2161-7290Ibrahim Ahmed Nur5https://orcid.org/0009-0004-6097-0102Abdikani Ali Hassan6https://orcid.org/0009-0006-9272-9529Venance Emmanuel Mswelo7https://orcid.org/0009-0009-9362-9943Department of Internal Medicine, Faculty of Clinical Medicine and Dentistry, Kampala International University, Ishaka, 20000, UgandaDepartment of Internal Medicine, Faculty of Clinical Medicine and Dentistry, Kampala International University, Ishaka, 20000, UgandaDepartment of Internal Medicine, Faculty of Clinical Medicine and Dentistry, Kampala International University, Ishaka, 20000, UgandaDepartment of Internal Medicine, Faculty of Clinical Medicine and Dentistry, Kampala International University, Ishaka, 20000, UgandaDepartment of Internal Medicine, Faculty of Clinical Medicine and Dentistry, Kampala International University, Ishaka, 20000, UgandaDepartment of Internal Medicine, Faculty of Clinical Medicine and Dentistry, Kampala International University, Ishaka, 20000, UgandaDepartment of Surgery, Faculty of Clinical Medicine and Dentistry, Kampala International University, Ishaka, 20000, UgandaDepartment of Internal Medicine, Faculty of Clinical Medicine and Dentistry, Kampala International University, Ishaka, 20000, UgandaSickle haemoglobin (HbS) is the most common abnormal haemoglobin mutation worldwide. In Uganda, according to the Uganda Sickle Surveillance Study (US3), the overall prevalence of sickle cell trait and disease is 13.3% and 0.7%, respectively. SCD presents with numerous complications. Acute Soft Head Syndrome (ASHS) or sickle cell cephalohematoma is among the rare complications of SCD. We report a 14-year-old adolescent male, a resident of rural Western Uganda, who presented with a history of non-traumatic painless scalp swelling for a week and multiple joints pain for 5 days. He had a similar swelling in the previous six months, which subsided after blood transfusion given at a nearby health facility. There was a history of on-and-off fever, easy fatiguability, and generalized body weakness. Complete blood counts revealed anemia, Haemoglobin Electrophoresis confirmed Sickle Cell Anemia. Head Computed Tomography concluded a subgaleal fluid collection. The diagnosis of acute soft head syndrome was established in a newly diagnosed SCD patient. This case highlights a rare diagnosis of acute soft head syndrome as well as a late diagnosis of SCD in adolescent in rural settings. In such settings, the pre-existing poor socio-economic background coupled with atypical presentation constitute a major impediment for timely diagnosis.https://qaaspa.com/index.php/bmtj/article/view/28acute soft head syndromesickle cell diseaserural
spellingShingle Abukar Ali Ahmed
Dalton Kambale Munyambalu
Awil Abdulkadir Abdi
Elias Joseph Xwatsal
Hanan Asad Hassan
Ibrahim Ahmed Nur
Abdikani Ali Hassan
Venance Emmanuel Mswelo
Acute Soft Head Syndrome as the Initial Presentation of Sickle Cell Disease in an Adolescent in Rural Western Uganda: Case Report
BioMed Target Journal
acute soft head syndrome
sickle cell disease
rural
title Acute Soft Head Syndrome as the Initial Presentation of Sickle Cell Disease in an Adolescent in Rural Western Uganda: Case Report
title_full Acute Soft Head Syndrome as the Initial Presentation of Sickle Cell Disease in an Adolescent in Rural Western Uganda: Case Report
title_fullStr Acute Soft Head Syndrome as the Initial Presentation of Sickle Cell Disease in an Adolescent in Rural Western Uganda: Case Report
title_full_unstemmed Acute Soft Head Syndrome as the Initial Presentation of Sickle Cell Disease in an Adolescent in Rural Western Uganda: Case Report
title_short Acute Soft Head Syndrome as the Initial Presentation of Sickle Cell Disease in an Adolescent in Rural Western Uganda: Case Report
title_sort acute soft head syndrome as the initial presentation of sickle cell disease in an adolescent in rural western uganda case report
topic acute soft head syndrome
sickle cell disease
rural
url https://qaaspa.com/index.php/bmtj/article/view/28
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