{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,30]],"date-time":"2025-07-30T14:09:47Z","timestamp":1753884587230,"version":"3.41.2"},"reference-count":0,"publisher":"SMC Media","issue":"Vol 7 No 4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:p>Isolated congenital asplenia is a rare condition that mostly manifests in the early years, usually due to fatal systemic infections. In this paper, however, we present a case of a 36-year-old asymptomatic patient who was referred for suspected hyposplenism, with no history of splenectomy. There were no significant changes on physical examination. Blood analysis revealed leukocytosis and thrombocytosis as well as moderate anisopoikilocytosis and red blood cells with Howell\u2013Jolly bodies. No spleen or other malformations were identified on imaging. Individuals with isolated congenital asplenia have an increased susceptibility to invasive infections and sepsis, with rapid clinical decline and a high mortality rate despite treatment.<\/jats:p>","DOI":"10.12890\/2020_001429","type":"journal-article","created":{"date-parts":[[2021,5,25]],"date-time":"2021-05-25T13:52:37Z","timestamp":1621950757000},"source":"Crossref","is-referenced-by-count":0,"title":["Isolated Congenital Asplenia in an Asymptomatic Patient: A Very Rare Diagnosis"],"prefix":"10.12890","author":[{"family":"Sofia Dinis Ferreira","sequence":"first","affiliation":[{"name":"Medicina Intensiva, Hospital Central do Funchal, SESARAM, Funchal, Madeira, Portugal"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"family":"Cl\u00e1udia Lemos","sequence":"additional","affiliation":[{"name":"Medicina Intensiva, Hospital Central do Funchal, SESARAM, Funchal, Madeira, Portugal"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"family":"M\u00f3nica Caldeira","sequence":"additional","affiliation":[{"name":"Medicina Interna, Hospital Central do Funchal, SESARAM, Funchal, Madeira, Portugal"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"family":"Miguel Homem da Costa","sequence":"additional","affiliation":[{"name":"Medicina Interna, Hospital Central do Funchal, SESARAM, Funchal, Madeira, Portugal"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"family":"Maria Luz Braz\u00e3o","sequence":"additional","affiliation":[{"name":"Medicina Interna, Hospital Central do Funchal, SESARAM, Funchal, Madeira, Portugal"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"family":"Fernando Aveiro","sequence":"additional","affiliation":[{"name":"Hematologia Cl\u00ednica, Hospital Central do Funchal, SESARAM, Funchal, Madeira, Portugal"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"10397","published-online":{"date-parts":[[2020,2,28]]},"container-title":["European Journal of Case Reports in Internal Medicine"],"original-title":[],"deposited":{"date-parts":[[2021,5,25]],"date-time":"2021-05-25T13:56:28Z","timestamp":1621950988000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ejcrim.com\/index.php\/EJCRIM\/article\/view\/1429"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,2,28]]},"references-count":0,"journal-issue":{"issue":"Vol 7 No 4","published-online":{"date-parts":[[2019]]}},"URL":"https:\/\/doi.org\/10.12890\/2020_001429","relation":{"has-manifestation":[{"id-type":"other","id":"1-57-1429-g1977","asserted-by":"subject"},{"id-type":"other","id":"1-57-1429-g1978","asserted-by":"subject"}],"is-part-of":[{"id-type":"other","id":"1-57","asserted-by":"subject"}]},"ISSN":["2284-2594"],"issn-type":[{"type":"electronic","value":"2284-2594"}],"subject":[],"published":{"date-parts":[[2020,2,28]]},"article-number":"6"}}