Search Results - "Derya Özyörük"

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  1. 1

    Ovarian Mucinous Carcinoma in a Pediatric Patient With Maroteaux-Lamy Syndrome by Yazal Erdem, Arzu, Özyörük, Derya

    Published in Journal of pediatric hematology/oncology (01-11-2021)
    “…Mucopolysaccharidoses (MPS) are autosomal recessive lysosomal storage disorder (LSD). Mucinous ovarian cancer is a rare tumor and seldom encounters among…”
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    Journal Article
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    The Development of Chylothorax in a Child With T-cell Lymphoblastic Lymphoma and Ataxia Telangiectasia During Induction Therapy by Özyörük, Derya, Güzelküçük, Zeliha, Hacisalihoglu, Şadan, Cinel, Güzin

    Published in Journal of pediatric hematology/oncology (01-03-2022)
    “…Chylothorax is an unusual complication of childhood cancer. It causes to additional morbidity and mortality during management. It should be kept in mind that…”
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    Journal Article
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    NEUROBLASTOMA AND ASSOCIATED DISORDERS, A SINGLE CENTER EXPERIENCE by Arzu Yazal Erdem, Selma Çakmakcı, Seda Şahin, Derya Özyörük, Neriman Sarı, Suna Emir, İnci Ergürhan İlhan

    Published in Hematology, Transfusion and Cell Therapy (01-10-2023)
    “…Objective: The genetic factors involved in development of neuroblastoma are not yet well understood. The most common somatic genomic alterations in…”
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    NUT Midline Carcinoma of the Lung in a Six-Year-Old Child by Karakuş, Esra, Poyraz, Aylar, Oğuz Erdogan, Ayşe Selcen, Emir, Suna, Özyörük, Derya

    Published in Fetal and pediatric pathology (02-11-2017)
    “…Background: Nuclear protein of the testis (NUT) midline carcinoma is genetically defined by rearrangement of NUT or by immunohistochemical expression of NUT…”
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    PROLONGED COVID-19 POSITIVITY AND CHEMOTHERAPY IN A PATIENT WITH NASOPHARENGEAL CARCINOMA by Şahin, Seda, Sarı, Neriman, Özyörük, Derya, Özdemir, Sonay İncesoy, Gülhan, Belgin, İlhan, İnci Ergürhan

    Published in Hematology, Transfusion and Cell Therapy (01-11-2021)
    “…Nasopharyngeal carcinoma is a rare tumor that accounts for 1-3% of all childhood malignancies. A 16-year-old patient with refractory nasopharyngeal carcinoma,…”
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    Eculizumab for bevacizumab induced thrombotic microangiopathy: A case report by İnözü, Mihriban, Özlü, Sare Gülfem, Özyörük, Derya, Kiremitçi, Saba, Çakmakçı, Selma, Avcı, Begüm, Özdemir, Sonay İncesoy, Bayrakçı, Umut Selda

    Published in Pediatric hematology oncology journal (01-12-2022)
    “…Bevacizumab is a monoclonal human antibody that is effective in the treatment of cancers in both adults and children due to inhibition of vascular endothelial…”
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    EVALUATION AND MANAGEMENT OF THYROID NODULES AT A TERTIARY CARE PEDIATRIC CANCER CENTER IN TURKEY by Seda Şahin, Derya Özyörük, Arzu Yazal Erdem, Neriman Sarı, Aylin Kılınç Uğurlu, Mehmet Boyrazoğlu, Selma Çakmakcı, İnci Ergürhan İlhan

    Published in Hematology, Transfusion and Cell Therapy (01-10-2022)
    “…Objective: The object of this study is to search the characteristics of children and adolescents with thyroid nodules and analyze our institutional experience…”
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  9. 9

    NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA by Arzu Yazal Erdem, Sonay İncesoy Özdemir, Meriç Kamak Cihan, Derya Özyörük, Neriman Sarı, İnci Ergürhan İlhan

    Published in Hematology, Transfusion and Cell Therapy (01-11-2021)
    “…Case report: The majority of neuroblastomas are sporadic and not correlated with any specific constitutional germline chromosomal abnormality, inherited…”
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    THREE CASES WITH BURKITT LYMPHOMA PRESENTING WITH CHOLESTASIS by Fatma Tuba YILDIRIM, Derya ÖZYÖRÜK, Arzu YAZAL ERDEM, Selma ÇAKMAKCI, Neriman SARI, Sonay İNCESOY, İnci İLHAN

    Published in Hematology, Transfusion and Cell Therapy (01-11-2021)
    “…Case report: Cholestasis secondary to neoplasm is rare in children. It is also rare in Burkitt lymphoma and may be cause to treatment delay. We report 3 cases…”
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    A CASE DIAGNOSED WITH FOUR DIFFERENT TUMORS by Fatma Tuba YILDIRIM, Derya ÖZYÖRÜK, Arzu YAZAL ERDEM, Selma ÇAKMAKCI, Neriman SARI, Sonay İNCESOY, İnci İLHAN

    Published in Hematology, Transfusion and Cell Therapy (01-11-2021)
    “…Case report: Chromosomal breakage syndromes are characterized by cancer predisposition. Here we present a 27-month-old female with Fanconi Aplastic Anemia…”
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    Squamous cell carcinoma associated with Xeroderma pigmentosum: an unusual presentation with a tremendously huge mass over the face and paraneoplastic hypercalcemia-hyperleukocytosis by Emir, Suna, Hacısalihoğlu, Şadan, Özyörük, Derya, Kaçar, Dilek, Erdem, Arzu, Karakuş, Esra

    Published in Turkish journal of pediatrics (2017)
    “…Emir S, Hacısalihoğlu Ş, Özyörük D, Kaçar D, Erdem A, Karakuş E. Squamous cell carcinoma associated with Xeroderma pigmentosum: an unusual presentation with a…”
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    Chronic lymphocytic leukemia in a child: A challenging diagnosis in pediatric oncology practice by Demir, Hacı Ahmet, Bayhan, Turan, Üner, Ayşegül, Kurtulan, Olcay, Karakuş, Esra, Emir, Suna, Özyörük, Derya, Ceylaner, Serdar

    Published in Pediatric blood & cancer (01-05-2014)
    “…Chronic lymphocytic leukemia/lymphoma (CLL) is an extremely rare disease during childhood. We report a 16‐year‐old female who presented with lymphadenopathies…”
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    Accidental cisplatin overdose in a child: Successful management with repetitive plasmapheresis and use of chemoprotective agents by Emir, Suna, Özyörük, Derya, Arman, Özlem, Özbek, Namık, Tunç, Bahattin

    Published in Turkish journal of pediatrics (2016)
    “…Cisplatin is one of the effective chemotherapeutic agents widely used for many tumor types in children. The most serious complications of cisplatin overdose…”
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    THE SMALLEST PRIMARY BONE LYMPHOMA by Fatma Burçin KURTİPEK, Volkan KÖSE, Seda ŞAHİN, Derya ÖZYÖRÜK, Neriman SARI, Sonay İNCESOY ÖZDEMİR, Arzu YAZAL ERDEM, Meriç KAYMAK, İnci İLHAN ERGÜRHAN

    Published in Hematology, Transfusion and Cell Therapy (01-11-2021)
    “…Case report: Primary lymphoma of bone (PLB) is a rare malignant condition with lymphocytic infiltration of the bone; it accounts for 2–3% of all primary bone…”
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    Journal Article
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    Occurrence of Wilms' tumor in a child with hereditary spherocytosis by Özyörük, Derya, Demir, Hacı Ahmet, Emir, Suna, Karakuş, Esra, Tunç, Bahattin

    Published in Turkish journal of pediatrics (01-03-2015)
    “…Hereditary spherocytosis (HS) is the most frequent cause of congenital hemolytic anemia. It is an autosomal dominant genetic disorder characterized by cell…”
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    Teratoid Wilms' Tumor Exhibiting Extensive Squamous Differentiation by Karaku, Esra, Senayli, Atilla, Özcan, Fatma, Demir, Ahmet Haci, Tiryaki, Tugrul, Özyörük, Derya, Emir, Suna

    Published in Fetal and pediatric pathology (01-02-2015)
    “…Teratoid Wilms' tumor is a rare renal tumor. Herein, we report an unusual variant of such tumor which simulated renal teratoma because of abundant keratinized…”
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    Primary Ovarian Malignant Melanoma Arising in Teratomatous Component of Mixed- Germ Cell Tumor in a Child: Case report by Özyörük, Derya, Demir, Hac Ahmet, Emir, Suna, Haberal, Asuman Nihan, Bugdayc, Meral, Ötgün, brahim

    Published in Pediatric hematology and oncology (01-05-2014)
    “…Primary ovarian malignant melanoma arising in teratomatous component of germ cell tumors is seen extremely rare with most reports being only of single cases…”
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