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  • Hematology Reports is published by MDPI from Volume 14 Issue 1 (2022). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with PAGEPress.

Hematology Reports, Volume 7, Issue 2

2015 June - 8 articles

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Articles (8)

  • Review
  • Open Access
29 Citations
1,343 Views
4 Pages

Hemocytometric parameters like red blood cell (RBC) count, mean red blood cell volume (MCV), reticulocyte count, red blood cell distribution width (RDW-SD) and zinc protoporphyrin (ZPP) are frequently established for discrimination between iron-defic...

  • Article
  • Open Access
8 Citations
1,075 Views
4 Pages

Prognostic Factors and Outcomes of Adult-Onset Hemophagocytic Lymphohistiocytosis: A Retrospective Analysis of 34 Cases

  • Masafumi Oto,
  • Kanako Yoshitsugu,
  • Shima Uneda,
  • Michiko Nagamine and
  • Minoru Yoshida

Adult-onset hemophagocytic lymphohistiocytosis (HLH) has features that are distinct from that of HLH in pediatric patients. The clinical records at the Japanese Red Cross Kumamoto Hospital were reviewed. We retrospectively analyzed 34 patients who fu...

  • Case Report
  • Open Access
21 Citations
741 Views
4 Pages

Differential Diagnosis of Isolated Myeloid Sarcoma: A Case Report and Review of the Literature

  • Patrick A. Hagen,
  • Charanjeet Singh,
  • Melissa Hart and
  • Anne H. Blaes

Myeloid sarcoma (MS) is a rare disease entity identified as a variety of manifestations defined by the occurrence of extramedullary myeloid cell masses with or without bone marrow involvement. This case describes an unusual presentation of isolated M...

  • Case Report
  • Open Access
11 Citations
819 Views
3 Pages

Chalazia Development in Multiple Myeloma: A New Complication Associated with Bortezomib Therapy

  • Charles Yun,
  • Nikhil Mukhi,
  • Valerie Kremer,
  • Roman Shinder,
  • Vaibhav Verma and
  • Olcay Batuman

Multiple myeloma (MM) is a neoplasm of plasma cells within the bone marrow. A major impact on improving survival in MM has been the use of the boronic acid-derived proteasome inhibitor bortezomib, a first-in-class selective inhibitor of the 26S prote...

  • Article
  • Open Access
9 Citations
891 Views
4 Pages

Favorable Event Free-Survival of High-Dose Chemotherapy followed by Autologous Hematopoietic Stem Cell Transplantation for Higher Risk Diffuse Large B-Cell Lymphoma in First Complete Remission

  • Hiroto Kaneko,
  • Yasuhiko Tsutsumi,
  • Takahiro Fujino,
  • Saeko Kuwahara,
  • Muneo Ohshiro,
  • Toshiki Iwai,
  • Junya Kuroda,
  • Shouhei Yokota,
  • Shigeo Horiike and
  • Masafumi Taniwaki

High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) has been applied to patients with diffuse large B-cell lymphoma (DLBCL); it is well established that ASCT shows significant survival benefits for chemosensitive relapse. H...

  • Case Report
  • Open Access
6 Citations
728 Views
3 Pages

A Difficult Case of Hodgkin Lymphoma with Differential Diagnosis of Tuberculosis and Sarcoidosis

  • Nilüfer Göknar,
  • Erkan Çakır,
  • Fatma Betül Çakır,
  • Ozgur Kasapcopur,
  • Gulcin Yegen,
  • Ahmet Hakan Gedik and
  • Faruk Oktem

We report here the case of a 14-year-old boy with history of fever, weight loss, and mediastinal lymphadenopathy. The clinical symptoms and laboratory findings mimicking tuberculosis and sarcoidosis complicated the diagnostic process. He was diagnose...

  • Case Report
  • Open Access
8 Citations
835 Views
3 Pages

Inflammatory Pseudotumor of the Spleen

  • Georgia McMahon,
  • Kirsty Rady and
  • Henry Miles Prince

Isolated splenic inflammatory pseudotumors (IPT) are extremely rare, typically benign, inflammatory lesions with varied clinical presentations that pose a diagnostic challenge to clinicians due to their similarity in appearance to neoplasms. We prese...

  • Case Report
  • Open Access
8 Citations
820 Views
4 Pages

Angioimmunoblastic T-cell lymphoma (AITL) is an aggressive peripheral T-cell lymphoma typically characterized by prominent lymphadenopathy and B-symptoms at the time of presentation, polyclonal hypergammaglobulinemia, autoimmune hemolysis and frequen...

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Hematol. Rep. - ISSN 2038-8330