Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Werlhof's disease"'
Autor:
Amel Zerroukhi, Martha Duraes, Julien Baleine, Jean-François Schved, Isabelle Cau-Diaz, Tarik Kanouni, Elodie Boissier, Olivier Dautremay, Lionel Moulis, Alexandre Theron, Eric Jeziorski, Christine Biron-Andreani, Michel Rodière
Publikováno v:
Blood Advances
Key Points IPF has a typical clinical presentation with involvement of the lower limbs corresponding to vascular territories.The antithrombin level and platelet count at diagnosis seemed to be associated with severe complications in IPF.
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Publikováno v:
Mìžnarodnij Endokrinologìčnij Žurnal, Vol 17, Iss 3, Pp 234-240 (2021)
This review summarizes data on the incidence of autoimmune diseases and examines the prevalence of antithyroid antibodies in extrathyroid autoimmune diseases. In the world, about 5–7 % of the population suffers from one or another type of autoimmun
Publikováno v:
Tatiane Fidelis da Silva Foltran
Neste estudo, objetivou-se tratar, por meio da terapia cognitivo-comportamental, o transtorno de ansiedade de pacientes que se encontram em tratamento médico, cujo diagnóstico é de púrpura idiopática. Para tanto, participaram, três pacientes, d
Publikováno v:
Postgraduate medical journal. 96(1138)
A 48-year-old diabetic woman presented with 2-day history of fever and skin discolouration over hand. On admission, her vital parameters were stable and systemic examination unremarkable. Cutaneous examination revealed well-defined dusky ecchymotic p
Autor:
Acw Lee
Publikováno v:
Journal of pediatric hematology/oncology. 41(1)
An acquired, transient bleeding disorder that predominantly affects children in Southeast Asia has been reported for the last 4 decades. The condition has been named idiopathic purpura with gray platelets (IPGP) or acquired platelet dysfunction with
Autor:
K. Mortaji, K. Khadir, F Lasry, H. Benchikhi, M. Itri, F. Fadil, Sellama Nadifi, Fz Elfatoiki, N. Sarbati
Publikováno v:
Archives de Pédiatrie. 20:499-502
The association of idiopathic purpura fulminans (PF) and venous thrombosis (VT) seldom reveals constitutional thrombophilia in an infant. We report a case of PF in an 18-month-old infant. Laboratory tests showed disseminated intravascular coagulation
Autor:
Meenal Patil, Vikas Karne
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 28:54-57
We report anaesthesia management of a parturient with severe thrombocytopenia secondary to immune thrombocytopenic purpura (ITP). Her platelet count remained around 3 × 109/l in spite of optimum medical therapy and hence was posted for splenectomy c
Publikováno v:
Hernia. 15:709-712
On the 3rd day following surgery to repair an incisional hernia, a 67-year-old male patient with Werlhof's disease (idiopathic thrombocytopenic purpura) was diagnosed with a histologically confirmed pyoderma gangraenosum (PG), a rare complication of
Autor:
Jesper Stentoft
Publikováno v:
British Journal of Haematology. 175:755-756