Pregled bibliografske jedinice broj: 1216544
Severe intracranial haemorrhage in neonatal alloimmune thrombocytopenia due to antibodies against human platelet antigen 1b: Case report and literature review
Severe intracranial haemorrhage in neonatal alloimmune thrombocytopenia due to antibodies against human platelet antigen 1b: Case report and literature review // Transfusion medicine, 32 (2022), 269-275 doi:10.1111/tme.12892 (međunarodna recenzija, članak, stručni)
CROSBI ID: 1216544 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Severe intracranial haemorrhage in neonatal
alloimmune thrombocytopenia due to antibodies
against human platelet antigen 1b: Case report and
literature review
Autori
Tomac, Gordana ; Gojčeta, Koraljka ; Grizelj, Ruža ; Coen Herak, Desiree ; Baršić Ostojić, Sanja ; Golubić Ćepulić, Branka
Izvornik
Transfusion medicine (0958-7578) 32
(2022);
269-275
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, stručni
Ključne riječi
anti-HPA-1b antibodies ; fetal/neonatal alloimmune thrombocytopenia ; intracranial haemorrhage
Sažetak
Fetal/neonatal alloimmune thrombocytopenia (FNAIT) is a rare life- threatening disorder, leading to severe thrombocytopenia and potentially bleeding, with intracranial haemorrhage (ICH) being the most serious complication. We report on a FNAIT case with fourth- degree ICH that arose due to antibodies against human platelet antigen (HPA)-1b. The male infant, born to an otherwise healthy mother, presented with severe signs of ICH soon after delivery. Since only moderate thrombocytopenia was noted and there were no active signs of bleeding, the infant did not receive intravenous immunoglobulins (IVIg) or platelet transfusion. Spontaneous recovery of platelets was noted on the eighth day of life, but permanent neurological impairment remained as a consequence of ICH. We report the results of HPA and human leukocyte antigen (HLA) antibodies in the mother's and the infant's sera, the family's HPA genotype and the mother's HLA genotype, and summarise previously described cases of FNAIT due to anti-HPA-1b antibodies in the literature. FNAIT with severe ICH due to anti-HPA-1b antibodies is rarely diagnosed. An association between HLA genes and sensitization to HPA-1b antibodies was not demonstrated. The severity of FNAIT and the occurrence of ICH is often difficult to predict. In this case, the infant presented with moderate thrombocytopenia and ICH, with subsequent permanent consequences.
Izvorni jezik
Engleski
Znanstvena područja
Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb,
Zdravstveno veleučilište, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE