{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T11:14:28Z","timestamp":1780917268359,"version":"3.54.1"},"reference-count":0,"publisher":"South African Medical Association NPC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["SAMJ"],"published-print":{"date-parts":[[2021,12,20]]},"abstract":"<jats:p>Patients with Gaucher disease (GD), a rare autosomal recessive lysosomal storage disease, commonly present to paediatricians with massive splenomegaly. While the diagnosis and management of patients with this chronic multisystem disorder has evolved significantly in recent years, the initial diagnosis represents a challenge. We describe the case of a 15-year-old black African male who presented with abdominal distension, delayed growth and fatigue. Initial laboratory studies revealed severe anaemia (haemoglobin concentration 8 g\/dL) and moderate thrombocytopenia (platelet count 80 \u00d7 109\/L). A computed tomography scan of the abdomen showed an enlarged liver of 173 mm and massive splenomegaly of 27 mm. The diagnosis of GD was confirmed by reduced beta-glucocerebrosidase activity and heterozygous mutations in the GBA1 gene. The patient was managed at a dedicated paediatric haematology unit with enzyme replacement therapy and regular clinical, biochemical and radiological monitoring.<\/jats:p>","DOI":"10.7196\/samj.2022.v112i1.16011","type":"journal-article","created":{"date-parts":[[2022,2,2]],"date-time":"2022-02-02T16:41:02Z","timestamp":1643820062000},"page":"17-20","source":"Crossref","is-referenced-by-count":0,"title":["Gaucher disease: A cause of massive splenomegaly in a 15-year-old black African male"],"prefix":"10.7196","author":[{"name":"Department of Paediatrics and Child Health, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9490-6916","authenticated-orcid":false,"given":"T","family":"Ramdin","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E","family":"Schapkaitz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S","family":"Varughese","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H","family":"Sevitz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"4425","published-online":{"date-parts":[[2021,12,20]]},"container-title":["South African Medical Journal"],"original-title":[],"deposited":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T10:37:33Z","timestamp":1780915053000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.co.za\/doi\/abs\/10.7196\/SAMJ.2022.v112i1.16011"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,12,20]]},"references-count":0,"URL":"https:\/\/doi.org\/10.7196\/samj.2022.v112i1.16011","relation":{},"ISSN":["0256-9574","2078-5135"],"issn-type":[{"value":"0256-9574","type":"print"},{"value":"2078-5135","type":"electronic"}],"subject":[],"published":{"date-parts":[[2021,12,20]]}}}