Long-Term Follow-Up of Adult Patients with Idiopathic Thrombocytopenic Purpura after Splenectomy

2011 ◽  
Vol 4 (3) ◽  
pp. 285-289 ◽  
Author(s):  
Marica Pavkovic ◽  
Slobodanka Trpkovska-Terzieva ◽  
Arif Latifi ◽  
Oliver Karanfilski ◽  
Lidija Cevreska ◽  
...  
Keyword(s):  
Idiopathic Thrombocytopenic Purpura ◽  
Adult Patients ◽  
Thrombocytopenic Purpura ◽  
Long Term Follow Up

Rituximab therapy in adult patients with relapsed or refractory immune thrombocytopenic purpura: long-term follow-up results

2008 ◽  
Vol 81 (3) ◽  
pp. 165-169 ◽  
Author(s):  
Marta Medeot ◽  
Francesco Zaja ◽  
Nicola Vianelli ◽  
Marta Battista ◽  
Michele Baccarani ◽  
...  
Keyword(s):  
Immune Thrombocytopenic Purpura ◽  
Adult Patients ◽  
Thrombocytopenic Purpura ◽  
Long Term Follow Up

scholarly journals P096 Long-term follow-up of adolescent and adult patients with cystic fibrosis: a single centre's experience

2021 ◽  
Vol 20 ◽  
pp. S68
Author(s):  
A.I. Yilmaz ◽  
G. Ünal ◽  
B.S. Kibar ◽  
P. Sevgi ◽  
O. Eĝil ◽  
...  
Keyword(s):  
Cystic Fibrosis ◽  
Adult Patients ◽  
Long Term Follow Up

Long-term Follow-up in Adult Patients with Cystic Fibrosis and Deep Intronic Splicing Variants

2021 ◽  
Vol 57 (7) ◽  
pp. 501-503
Author(s):  
Antonio Álvarez ◽  
Karina Loor ◽  
Paula Fernández-Alvarez ◽  
Silvia Gartner ◽  
Eva Polverino ◽  
...  
Keyword(s):  
Cystic Fibrosis ◽  
Adult Patients ◽  
Splicing Variants ◽  
Long Term Follow Up

Long-term follow-up of dysphagia in adult patients with Duchenne muscular dystrophy

2018 ◽  
Vol 22 (5) ◽  
pp. 786-790 ◽  
Author(s):  
Yuka Yamada ◽  
Michiyuki Kawakami ◽  
Ayako Wada ◽  
Shogo Fukui ◽  
Koshiro Haruyama ◽  
...  
Keyword(s):  
Duchenne Muscular Dystrophy ◽  
Muscular Dystrophy ◽  
Adult Patients ◽  
Long Term Follow Up

ANAPHYLACTOID PURPURA (SCHÖNLEIN-HENOCH SYNDROME)

PEDIATRICS ◽  
1955 ◽  
Vol 16 (2) ◽  
pp. 196-206
Author(s):  
Ralph J. P. Wedgwood ◽  
Marshall H. Klaus
Keyword(s):  
Renal Disease ◽  
Acute Phase ◽  
Chronic Renal Disease ◽  
Average Length ◽  
Adult Patients ◽  
Follow Up Study ◽  
Long Term Follow Up

A long-term follow-up study of 26 children with anaphylactoid purpura (Schönlein-Henoch Syndrome) is presented. The average length of follow-up was 4½ years. Of these 26 children, 10 were found to have an apparent latent nephritis characterized by hematuria and cylinduria, but without marked proteinuria. Nine of the ten children were over the age of 6 years at the time of onset of purpura; 6 had proteinuria or hematuria during the acute phase of the disease. It is suggested that this renal sequela of anaphylactoid purpura may constitute one of the origins of chronic renal disease "of unknown etoiology" which occurs in adult patients.

Long-term follow-up of 103 untreated adult patients with type 1 Gaucher disease

2019 ◽  
Vol 126 (2) ◽  
pp. S49
Author(s):  
Tama Dinur ◽  
Ari Zimran ◽  
Michal Becker Cohen ◽  
David Arkadir ◽  
Claudia Cozma ◽  
...  
Keyword(s):  
Gaucher Disease ◽  
Adult Patients ◽  
Long Term Follow Up ◽  
Type 1 Gaucher Disease

scholarly journals A Case of Pregnancy Complicated with Evans Syndrome with Sequential Development of Autoimmune Warm Antibody Hemolytic Anemia and Idiopathic Thrombocytopenic Purpura

2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Haruka Suzuki ◽  
Koji Yamanoi ◽  
Jumpei Ogura ◽  
Takahiro Hirayama ◽  
Koji Yasumoto ◽  
...  
Keyword(s):  
Hemolytic Anemia ◽  
Idiopathic Thrombocytopenic Purpura ◽  
Macrocytic Anemia ◽  
Evans Syndrome ◽  
Thrombocytopenic Purpura ◽  
Sequential Development ◽  
Healthy Female ◽  
Long Term Follow Up ◽  
Haptoglobin Level

The simultaneous or sequential development of autoimmune hemolytic anemia (AIHA) and idiopathic thrombocytopenic purpura (ITP) is known as Evans syndrome. We experienced a case of Evans syndrome that developed AIHA during pregnancy and ITP long after delivery. The patient was a 35-year-old pregnant woman (gravida 2, para 1). A routine blood test at 28 weeks of gestation revealed moderate macrocytic anemia. Her haptoglobin level was markedly low, and a direct antiglobulin test (DAT) was positive. Based on these results, AIHA was considered. A healthy female newborn with bodyweight 3575 g was vaginally delivered uneventfully. After delivery, the DAT remained positive, but anemia did not develop. At 203 days after delivery, ITP was detected. Because AIHA and ITP developed sequentially, she was diagnosed with Evans syndrome. When AIHA occurs during pregnancy, long-term follow-up is needed because ITP can develop sequentially.

Long‐term follow‐up of adult patients with congenital heart disease and an implantable cardioverter defibrillator

2019 ◽  
Vol 14 (4) ◽  
pp. 525-533 ◽  
Author(s):  
Madalena Coutinho Cruz ◽  
André Viveiros Monteiro ◽  
Guilherme Portugal ◽  
Sérgio Laranjo ◽  
Ana Lousinha ◽  
...  
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Implantable Cardioverter Defibrillator ◽  
Congenital Heart ◽  
Adult Patients ◽  
Cardioverter Defibrillator ◽  
Long Term Follow Up
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