Dergiler / Turkish Journal of Hematology / 2018 / Cilt: 35 - Sayı: 2

Safra Kesesinin İntravasküler Diffüz Büyük Hücreli Lenfoması

Intravascular Large B-Cell Lymphoma of the Gallbladder

Sayfa
145–146
Yayın Tarihi
2022-11-05
DOI
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Abstract

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Bu Makaleye Atıf Yap

AKYÜREK, N., ÖZET, A., KARACA, F., ÇETİN, B., METİN, Y., BİLGETEKİN, İ. (2022). Safra Kesesinin İntravasküler Diffüz Büyük Hücreli Lenfoması. Turkish Journal of Hematology, Cilt: 35 - Sayı: 2, 145–146. https://ajindex.com/articles/606754

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Kaynakça (5)

  1. Shimazaki C, Inaba T, Nakagawa M. B-cell lymphoma-associated hemophagocytic syndrome. Leuk Lymphoma 2000;38:121-130
  2. Murase T, Nakamura S, Kawauchi K, Matsuzaki H, Sakai C, Inaba T, Nasu K, Tashiro K, Suchi T, Saito H. An Asian variant of intravascular large B-cell lymphoma: clinical, pathological and cytogenetic approaches to diffuse large B-cell lymphoma associated with haemophagocytic syndrome. Br J Haematol 2000;111:826-834
  3. Murase T, Nakamura S. An Asian variant of intravascular lymphomatosis: an updated review of malignant histiocytosis-like B-cell lymphoma. Leuk Lymphoma 1999;33:459-473
  4. Ferreri AJ, Dognini GP, Campo E, Willemze R, Seymour JF, Bairey O, Martelli M, De Renz AO, Doglioni C, Montalbán C, Tedeschi A, Pavlovsky A, Morgan S, Uziel L, Ferracci M, Ascani S, Gianelli U, Patriarca C, Facchetti F, Dalla Libera A, Pertoldi B, Horváth B, Szomor A, Zucca E, Cavalli F, Ponzoni M; International Extranodal Lymphoma Study Group (IELSG). Variations in clinical presentation, frequency of hemophagocytosis and clinical behavior of intravascular lymphoma diagnosed in different geographical regions. Haematologica 2007;92:486-492
  5. Ferreri AJ, Campo E, Seymour JF, Willemze R, Ilariucci F, Ambrosetti A, Zucca E, Rossi G, López-Guillermo A, Pavlovsky MA, Geerts ML, Candoni A, Lestani M, Asioli S, Milani M, Piris MA, Pileri S, Facchetti F, Cavalli F, Ponzoni M; International Extranodal Lymphoma Study Group (IELSG). Intravascular lymphoma: clinical presentation, natural history, management and prognostic factors in a series of 38 cases, with special emphasis on the “cutaneous variant.” Br J Haematol 2004;127:173-183.