Glanzmann thrombasthenia presenting with corpus luteum hemorrhagicum: A case report "Corpus luteum hemorrhagicum" ile ortaya çikan Glanzmann trombastenisi: Olgu sunumu
Gulhane Medical Journal, cilt.49, sa.1, ss.49-51, 2007 (Scopus, TRDizin)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 49 Sayı: 1
- Basım Tarihi: 2007
- Dergi Adı: Gulhane Medical Journal
- Derginin Tarandığı İndeksler: Scopus, TR DİZİN (ULAKBİM)
- Sayfa Sayıları: ss.49-51
- Anahtar Kelimeler: Corpus luteum hemorrhagicum, Glanzmann thrombasthenia
- Sağlık Bilimleri Üniversitesi Adresli: Evet
Özet
Glanzmann thrombasthenia is a rare autosomal recessive disorder of platelet function that is characterized by prolonged bleeding time, and normal platelet count and morphology. It is caused by the deficiency or abnormality of the platelet glycoprotein IIb-IIIa. Thrombastenia is typically diagnosed by mucocutaneous bleeding in neonatal or infantile period. In further ages, common clinical manifestations include epistaxis, gingival bleeding, menorrhagia, gastrointestinal bleeding and hematuria. An unusual case of Glanzmann thrombasthenia who initially presented with "corpus luteum hemorrhagicum" is reported herein. © Gülhane Askeri Tip Akademisi 2007.