Browsing by Author "Çil T."
Now showing items 1-13 of 13
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Adult langerhans cell histiocytosis: Differential diagnosis
Çil T.; Gökalp D.; Tuzcu A.; Işikdoğan A.; Bahçeci M. (Turkiye Klinikleri, 2007)Langerhans cell histiocytosis is a group of idiopathic disorders characterized by the abnormal proliferation of specialized bone marrow-derived Langerhans cells. There are one to two cases per million population. Most ... -
Cancer and thrombotic thrombocytopenic purpura: Presentation of two cases
Altintaş A.; Çil T.; Atay A.E.; Kaplan M.A.; Işikdoğan A.; Ayyildiz O. (Turkiye Klinikleri, 2008)Thrombotic thrombocytopenic purpura (TTP) is a rare and fatal disease characterized by microangiopathic hemolytic anemia, thrombocytopenia, neurologic disorder, renal function deterioration and fever. TTP may be idiopathic ... -
Cladribine treatment outcomes of hairy cell leukemia
Altintaş A.; Ayyildiz O.; Atay A.E.; Çil T.; Müftüoğlu E. (2006)Hairy cell leukemia is a rare, clonal, chronic B cell lenfoproliferative disease characterized by splenomegaly and pancytopenia. Purine analogues are first-line choice of therapy. Although effectivity of treatment is ... -
Cranial involvement in a follicular lymphoma patient with systemic complete remission after Yttrium-90-ibritumomab-tiuxetan treatment: Scientific letter
Çil T.; Altintaş A.; Paşa S.; Kilinç I.; Işikdoğan A. (Turkiye Klinikleri, 2008)Non-Hodgkin's lymphoma is a heterogeneous group of lymphoproliferative disorders with varying patterns of behavior and treatment responses. Advances in understanding of tumor biology have made it possible to exploit novel ... -
Differential diagnosis of Churg Strauss syndrome: Two cases reports
Altintaş A.; Çil T.; Ayyildiz O.; Şit D.; Müftüoğlu E. (2007)Churg-Strauss syndrome (CSS) is characterized by necrotising, eosinophilic-rich granulomatous inflammation of small and medium vessels. Differantial diagnosis with Hypereosinophilic syndrome is crucial. Herein, we presented ... -
Gastric ring cell carcinoma metastasis to the breast: Two case reports
Çil T.; Altintaş A.; Paşa S.; Işikdoğan A. (2009)Metastatic tumors of breast are rare and account only for approximately 2% of all malignant breast cancers. Breast metastasis of stomach's signet ring cell carcinoma (SRCC) is also a very rare condition. Herein, we report ... -
Hepatitis B virus infection in patient with Hodgkin's and non-Hodgkin's lymphoma and clinical significance
Altintaş A.; Kaplan M.A.; Çil T.; Yilmaz Ş.; Bayan K.; Daniş R.; Ayyildiz O. (2007)Hepatitis B virus (HBV) is a hepatotrophic virus that have also a potential to replicate in lymphoid cells. This has led to evaluation of potential association between HBV infection and lymphomas. In this study, we ... -
Hereditary thrombophilic risk factors in patients with deep venous thrombosis
Altintaş A.; Çil T.; Kaplan M.A.; Yurt M.; Batun S. (2007)The prevalence of hereditary risk factors for deep venous thrombosis (DVT) varies greatly in different parts of the world. Factor V Leiden (FVL) and prothrombin G 20210A (FT G20210A) are the most common genetic defects ... -
Inhibitors in hemophilia A and B in Southeast of Turkey
Altintaş A.; Ayyildiz O.; Çil T.; Söker M.; Müftüoğlu E. (2006)Hemophilia A and B are inherited, X chromosome linked coagulation disorders that characterized by clinical signs and symptoms seen in males. The most important treatment related complication was viral infection in the past ... -
Patients with Hodgkin's disease: Clinical and pathological evaluation
Altintaş A.; Çil T.; Kaplan M.A.; Atay A.E.; Işikdoğan A.; Büyükbayram H.; Ayyildiz O. (2006)Hodgkins' disease accounts 25% of all lymphoid malignancies and 1% of all cancers. In this study, 150 patients with Hodgkins' disease were reviewed retrospectively and compared according to age, gender, histopathologic ... -
Splenectomy in lymphoproliferative disorders
Altintaş A.; Çil T.; Ayyildiz O. (2006)Splenomegaly is common in the course of lymphoproliferative disorders. Massive splenomegaly sometimes leads to bulk symptoms and cytopenias. Splenomegaly may also be the primary manifestation of lymphoproliferative disorders. ... -
Thrombotic thrombocytopenic purpura associated with Graves' disease
Altintaş A.; Çil T.; Ayyildiz O.; Kaplan M.A.; Müftüoğlu E. (2007)Thrombotic thrombocytopenic purpura (TTP) is characterized by microangiopathic hemolytic anemia and thrombocytopenia, usually accompanied by fever, renal failure and neurological deficits. TTP usually occurs in previously ... -
An unusual case of fever of unknown origin: Kikuchi-Fujimoto disease
Kikuchi-Fujimoto disease (KFD), also called histiositic necrotizing lenfadenitis is a self limited disease, which commonly affects young Asian women. Etiology of KFD is unknown. The disease presents with lymphadenopathy, ...
