Evidence map›Paper›PMID 38850017›Full record

ArticleThe American journal of case reports2024

Clinical Progression and Manifestations of H Syndrome: A Case Report of Failed Treatment Option.

Mohammed Al-Haddab, Fatimah J Al Muqarrab, Ahmed Alhumidi, Maha Alkofide

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Article in The American journal of case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Mohammed Al-HaddabDepartment of Dermatology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Fatimah J Al MuqarrabDepartment of Dermatology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.ORCID 0000-0002-0334-6547
Ahmed AlhumidiDepartment of Pathology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Maha AlkofideDepartment of Dermatology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND H syndrome is an autosomal recessive disorder of histiocytic proliferation with clinical spectrum of unique cutaneous and systemic manifestations. There is no consistent treatment for the disease, and all available options are based on case reports. Here, we present the chronological progression of a case of H syndrome with typical cutaneous manifestations that was misdiagnosed early as meningitis-induced sensorineural hearing loss and later as a non-defined autoimmune connective tissue disease. A new tried, although failed, treatment option is described as well. CASE REPORT A 31-year-old Saudi woman born of a consanguineous marriage presented to our dermatology clinic with symmetrical indurated hyperpigmented to violaceous plaques over the medial thighs, upper legs, lower back, volar wrists, and upper arms, associated with hypertrichosis. Hallux valgus of the big toes was clinically detected as well. She had a history of sensorineural deafness, diabetes mellitus, chronic anemia, and hypothyroidism. Genetic analysis of the patient showed a homozygous frameshift pathogenic variant of the SLC29A3 gene, c.243del p.(Lys81Asnfs*20). Systemic treatments in the form of methotrexate and imatinib had been tried; however, both failed to control her sclerotic cutaneous changes. CONCLUSIONS Knowing the early life presentation and the variable clinical symptoms of H syndrome is crucial in early intervention and further prevention of the non-reversible changes. Moreover, avoiding unnecessary immunosuppressive medication use is warranted in certain circumstances.

Indexed as

Hearing Loss, SensorineuralAdultContractureDisease ProgressionFemaleHistiocytosisHumansNucleoside Transport ProteinsTreatment FailureNucleoside Transport ProteinsSLC29A3 protein, human

Identifiers

PMID38850017
PMCPMC11176275

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