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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 9, Issue 1

February 2017 - 10 articles

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Articles (10)

  • Case Report
  • Open Access
2 Citations
681 Views
3 Pages

A 80-Year-Old Woman with B-Cell Prolymphocytic Leukemia

  • Alparslan Merdin,
  • Jale Yildiz,
  • Mehmet Sinan Dal,
  • Merih Kızıl Çakar,
  • Hikmetullah Batgi,
  • Emre Tekgündüz,
  • Aykut Onursever and
  • Fevzi Altuntaş

22 March 2017

Prolymhocytic leukemia (PLL) is a rare subtype of lymphocytic leukemias and its cells are immature lymphocytes. It is divided into 2 subgroups: T-PLL and B-PLL according to the lymphocytic origin of the cells. Discriminating B-PLL from other diseases...

  • Case Report
  • Open Access
7 Citations
753 Views
4 Pages

An Unusual Case of Primary Extranodal Lymphoma of the Gallbladder

  • Roberto Pezzuto,
  • Davide Di Mauro,
  • Luca Bonomo,
  • Amita Patel,
  • Edoardo Ricciardi,
  • Andrea Attanasio and
  • Antonio Manzelli

22 March 2017

Primary gallbladder lymphoma is an extremely rare disease. We report a case of a 63 year-old woman who has been admitted with gradual onset abdominal pain in the upper right quadrant and in the suprapubic region, nausea and malaise. According to the...

  • Case Report
  • Open Access
875 Views
3 Pages

Paroxysmal Nocturnal Hemoglobinuria in the Differential Diagnosis of Thrombocytopenia

  • Fusun Gediz,
  • Bahriye Kadriye Payzin,
  • Ozlem Zekiye Cakmak,
  • Yusuf Uzum,
  • Damla Ernur and
  • Fahri Sahin

22 March 2017

Paroxysmal nocturnal hemoglobinuria (PNH) is a disease which diagnosis may be delayed due to variable clinical findings. We describe herein a case of PNH in a 21 year old woman who admitted with complaints of chronic weakness, intermittent spontaneou...

  • Case Report
  • Open Access
9 Citations
751 Views
4 Pages

A Fatal Case of Immune Hyperhemolysis with Bone Marrow Necrosis in a Patient with Sickle Cell Disease

  • Matthew S. Karafin,
  • Arun Singavi,
  • Susan T. Johnson and
  • Joshua J. Field

In patients with sickle cell disease, hyperhemolysis is a rare but life-threatening complication of transfusion. In this case report, we describe a 61 year-old woman with hemoglobin sickle cell (SC) disease and history of alloimmunization who develop...

  • Case Report
  • Open Access
1 Citations
686 Views
3 Pages

Hemoglobin Willamette (b51 Pro → Arg): Case Report and Literature Review

  • Orivaldo Alves Barbosa,
  • Matheus Martins de Sousa Dias,
  • Saymon Medeiros Távora,
  • Gentil Claudino de Galiza Neto,
  • Jacqueline Holanda de Souza and
  • Herivaldo Ferreira da Silva

We report a case of hemoglobin (Hb) Willamette (β51 Pro → Arg) in the Hematology Department of a tertiary hospital in Fortaleza, Northeast of Brazil. A literature review of the cases described in health sciences databases using as a descriptor Hb Wil...

  • Case Report
  • Open Access
2 Citations
688 Views
4 Pages

Here we present the case of a 57-years old patient affected by hemophagocytic lymphohistiocytosis (HLH), a rare disease characterized by an uncontrolled immune activation, resulting in clinical and biochemical manifestations of extreme inflammation....

  • Article
  • Open Access
3 Citations
1,067 Views
6 Pages

The Efficacy of Colchicine and Dapsone Combination Therapy in Relapsed Immune Thrombocytopenia

  • Thanawat Rattanathammethee,
  • Wasan Theerajangkhaphichai,
  • Ekarat Rattarittamrong,
  • Sasinee Hantrakool,
  • Chatree Chai-Adisaksopha,
  • Lalita Norasetthada and
  • Adisak Tantiworawit

23 February 2017

The aim of the present paper is to evaluate the efficacy and safety of colchicine and dapsone combination therapy in cases of steroid-dependent, relapsed and refractory immune thrombocytopenia (ITP). This is a retrospective study of ITP patients who...

  • Case Report
  • Open Access
5 Citations
717 Views
4 Pages

Successful Intrathecal Chemotherapy Combined with Radiotherapy Followed by Pomalidomide and Low-Dose Dexamethasone Maintenance Therapy for a Primary Plasma Cell Leukemia Patient

  • Yusuke Yamashita,
  • Shinobu Tamura,
  • Takehiro Oiwa,
  • Hiroshi Kobata,
  • Kodai Kuriyama,
  • Toshiki Mushino,
  • Shogo Murata,
  • Hiroki Hosoi,
  • Akinori Nishikawa and
  • Nobuyoshi Hanaoka
  • + 1 author

23 February 2017

Primary plasma cell leukemia (PPCL) is a rare aggressive variant of plasma cell disorder and frequently presents with extramedullary disease. Central nervous system (CNS) involvement with PPCL has an extremely poor prognosis. We describe a 46-year-ol...

  • Article
  • Open Access
28 Citations
1,014 Views
3 Pages

23 February 2017

The aim of this study was to search for any relations between the neutrophil-tolymphocyte ratio (NLR) and the development of osteomyelitis and the need for amputation in patients with diabetic foot infection (DFI). All data included DFI patients who...

  • Brief Report
  • Open Access
28 Citations
2,016 Views
3 Pages

Impact of CRAB Symptoms in Survival of Patients with Symptomatic Myeloma in Novel Agent Era

  • Aya Nakaya,
  • Shinya Fujita,
  • Atsushi Satake,
  • Takahisa Nakanishi,
  • Yoshiko Azuma,
  • Yukie Tsubokura,
  • Masaaki Hotta,
  • Hideaki Yoshimura,
  • Kazuyoshi Ishii and
  • Tomoki Ito
  • + 1 author

23 February 2017

The acronym CRAB summarizes the most typical clinical manifestations of multiple myeloma, these being hypercalcemia, renal failure, anemia, and bone disease. CRAB can be used to distinguish between active, symptomatic multiple myeloma and monoclonal...

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Hematol. Rep. - ISSN 2038-8330Creative Common CC BY license