Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease

Immune thrombocytopenia is an autoimmune hematological disorder characterized by severely decreased platelet count of peripheral cause: platelet destruction via antiplatelet antibodies which may also affect marrow megakaryocytes. Patients may present in critical situations, with cutaneous and/or muc...

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Main Authors: Onisâi Minodora, Vlădăreanu Ana-Maria, Spînu Andreea, Găman Mihaela, Bumbea Horia
Format: Article
Language:English
Published: Sciendo 2019-12-01
Series:Romanian Journal of Internal Medicine
Subjects:
Online Access:https://doi.org/10.2478/rjim-2019-0014
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author Onisâi Minodora
Vlădăreanu Ana-Maria
Spînu Andreea
Găman Mihaela
Bumbea Horia
author_facet Onisâi Minodora
Vlădăreanu Ana-Maria
Spînu Andreea
Găman Mihaela
Bumbea Horia
author_sort Onisâi Minodora
collection DOAJ
description Immune thrombocytopenia is an autoimmune hematological disorder characterized by severely decreased platelet count of peripheral cause: platelet destruction via antiplatelet antibodies which may also affect marrow megakaryocytes. Patients may present in critical situations, with cutaneous and/or mucous bleeding and possibly life-threatening organ hemorrhages (cerebral, digestive, etc.) Therefore, rapid diagnosis and therapeutic intervention are mandatory.
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spelling doaj.art-289e14c6ec9c494e8362802c6f6eea122022-12-22T03:03:10ZengSciendoRomanian Journal of Internal Medicine2501-062X2019-12-0157427328310.2478/rjim-2019-0014rjim-2019-0014Idiopathic thrombocytopenic purpura (ITP) – new era for an old diseaseOnisâi Minodora0Vlădăreanu Ana-Maria1Spînu Andreea2Găman Mihaela3Bumbea Horia4Hematology Clinic, Emergency University Hospital, Bucharest, RomaniaHematology Clinic, Emergency University Hospital, Bucharest, RomaniaHematology Clinic, Emergency University Hospital, Bucharest, RomaniaHematology Clinic, Emergency University Hospital, Bucharest, RomaniaHematology Clinic, Emergency University Hospital, Bucharest, RomaniaImmune thrombocytopenia is an autoimmune hematological disorder characterized by severely decreased platelet count of peripheral cause: platelet destruction via antiplatelet antibodies which may also affect marrow megakaryocytes. Patients may present in critical situations, with cutaneous and/or mucous bleeding and possibly life-threatening organ hemorrhages (cerebral, digestive, etc.) Therefore, rapid diagnosis and therapeutic intervention are mandatory.https://doi.org/10.2478/rjim-2019-0014itpphysiopathologydiagnosistreatmentpregnancy
spellingShingle Onisâi Minodora
Vlădăreanu Ana-Maria
Spînu Andreea
Găman Mihaela
Bumbea Horia
Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease
Romanian Journal of Internal Medicine
itp
physiopathology
diagnosis
treatment
pregnancy
title Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease
title_full Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease
title_fullStr Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease
title_full_unstemmed Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease
title_short Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease
title_sort idiopathic thrombocytopenic purpura itp new era for an old disease
topic itp
physiopathology
diagnosis
treatment
pregnancy
url https://doi.org/10.2478/rjim-2019-0014
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AT gamanmihaela idiopathicthrombocytopenicpurpuraitpneweraforanolddisease
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