en POLSKI
eISSN: 2300-8660
ISSN: 0031-3939
Pediatria Polska - Polish Journal of Paediatrics
Current issue Archive Manuscripts accepted About the journal Editorial board Abstracting and indexing Contact Instructions for authors Ethical standards and procedures
Editorial System
Submit your Manuscript
SCImago Journal & Country Rank
2/2023
vol. 98
 
Share:
Share:
abstract:
Case report

Acquired thrombotic thrombocytopaenic purpura of an atypical, oligosymptomatic course in an adolescent girl – case report

Grażyna Waśka
1
,
Weronika Fijałkowska
1
,
Marta Badeńska
2
,
Andrzej Badeński
2
,
Agnieszka Książek
3
,
Renata Tomaszewska
3
,
Elżbieta Trembecka-Dubel
2
,
Maria Szczepańska
2

  1. Student at Department of Paediatrics, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, Poland
  2. Department of Paediatrics, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, Poland
  3. Department of Paediatric, Haematology, and Oncology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, Poland
Pediatr Pol 2023; 98 (2): 170-175
Online publish date: 2023/06/06
View full text Get citation
 
PlumX metrics:
Acquired thrombotic thrombocytopaenic purpura (TTP) in children is a rare immune-mediated haematological disease (iTTP) in which active thrombus formation and multiorgan symptoms resulting from ischaemia of specific organs occurs. A 16-year-old girl was admitted to the hospital with symptoms of haemorrhagic diathesis. Physical examination showed numerous small petechiae all over her body. Laboratory tests revealed thrombocytopaenia, increased parameters of inflammation, lactate dehydrogenase activity, and total bilirubin. Decreased a disintegrin and metalloproteinase with thrombospondin motifs, member 13 (ADAMTS-13) activity, and the ADAMTS-13 inhibitor were detected. At first, the symptoms were not specific enough, therefore initially some difficulties establishing a proper diagnosis occurred. Finally, the patient was diagnosed with primary autoimmune thrombocytopaenia and then underwent an adequate therapy with fresh frozen plasma (plasmapheresis and multiple infusions) combined with corticosteroids, which induced a sustained remission of the disease. The authors aimed to raise the awareness of the iTTP, especially with limited characteristic features, as presented, and highlight the significance of differential diagnosis.
keywords:

children, ADAMTS-13, acquired thrombotic thrombocytopaenic purpura, oligosymptomatic

 
Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.