Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Sarcoidosis-like Skin Lesions as the First Manifestation of Ataxia-Telangiectasia

Bibliographic Data

ID15718230
AuthorsBorko Milanović (0009-0002-4568-3450, Institute of Public Health of Vojvodina), Gordana Vijatov-Djuric (Institute of Public Health of Vojvodina), Andrea Djuretic (Institute of Public Health of Vojvodina), Jelena Kesić (0000-0001-9407-0568, Institute of Public Health of Vojvodina), Vesna Stojanović (0000-0003-4917-8961, University of Novi Sad), Milica Jaric (0000-0002-7639-0063, Institute of Public Health of Vojvodina), Ognjen Ležakov (0009-0007-0354-0458, Institute of Public Health of Vojvodina, corresponding author)
Year2025
Volume12
Issue6
Pages672-672
Publication date2025-05-23
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children12060672
PMID40564629
OpenAlexW4410639913
LanguageEN
References cited13

Ataxia-telangiectasia is a rare autosomal recessive disorder that is difficult to diagnose due to its unpredictable presentation. It is characterized by cerebellar degeneration, telangiectasias, immunodeficiency, frequent pulmonary infections, and tumors. Immune system abnormalities manifest as disruptions in both cellular and humoral immunity. The most common findings include decreased levels of immunoglobulin classes (IgA, IgM, IgG, and IgG subclasses) and a reduced number of T and B lymphocytes. A four-year-old girl was initially evaluated and treated for skin lesions that presented as crusts spreading across her body. She was monitored by a pulmonologist due to frequent bronchial obstructions. Over time, she developed bilateral scleral telangiectasia, saccadic eye movements, and impaired convergence. Her gait was wide-based and unstable, with truncal ataxia and a positive Romberg sign. Laboratory tests revealed decreased immunoglobulin G levels, subclass IgG4 levels, elevated alpha-fetoprotein, and a reduced number of T and B lymphocytes. Brain magnetic resonance imaging showed cerebellar atrophy. Whole-exome sequencing identified heterozygous variants c.1564-165del, p.(Glu5221lefsTer43), and c.7630-2A>C in the serine/threonine-protein kinase ATM (ataxia-telangiectasia mutated) gene, confirming the diagnosis of ataxia-telangiectasia. Following diagnosis, treatment with intravenous immunoglobulin replacement was initiated along with infection prevention and management. The goal of this case report is to raise awareness of the atypical initial presentation that may lead to a diagnostic delay. We emphasize the importance of considering ataxia-telangiectasia in the differential diagnosis, even when classical neurological signs are not yet evident

Ataxia · Ataxia-telangiectasia · Biology · Pathology · Sarcoidosis · Telangiectasia · Autoimmune Neurological Disorders and Treatments · DNA Repair Mechanisms · Genetic Neurodegenerative Diseases · Medicine · Dermatology

Highly citedNo

Tools

Open DOIOpen Access
Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae