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About 5,988 results

ALLMedicine™ Splenomegaly Center

Research & Reviews  2,955 results

A wandering spleen, splenomegaly, hypersplenism, and iron deficiency anaemia.
https://doi.org/10.1016/S0140-6736(20)31552-X
Lancet (London, England); Pouchot J, Couprie A

Aug 10th, 2020 - A wandering spleen, splenomegaly, hypersplenism, and iron deficiency anaemia.|2020|Pouchot J,Couprie A,|

A mutation in NOTCH2 gene first associated with Hajdu-Cheney syndrome in a Greek family...
https://doi.org/10.1007/s12020-020-02446-7
Endocrine Efstathiadou ZA, Kostoulas C et. al.

Aug 8th, 2020 - Hajdu-Cheney Syndrome (HCS) is a rare genetic autosomal dominant disorder, characterized by distinctive facial features, acroosteolysis, and severe osteoporosis. Very rarely HCS is associated with polycystic kidney disease, splenomegaly or Crohn's...

Bone lesions in hairy cell leukemia: Diagnosis and treatment.
https://doi.org/10.1111/ejh.13505
European Journal of Haematology; Robak P, Jesionek-Kupnicka D et. al.

Aug 4th, 2020 - Skeletal involvement is a rare complication of hairy cell leukemia (HCL) with an incidence of approximately 3%. Bone lesions are commonly lytic and the most common sites of involvement are the femoral head and neck. Skeletal involvement is typical...

The prognostic value and non-invasive predictors of splenomegaly in cirrhotic patients ...
https://doi.org/10.17219/acem/81935
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University; Zhou L, Wang SB et. al.

Aug 3rd, 2020 - The prognostic value and non-invasive predictors of splenomegaly in cirrhotic patients with hepatocellular carcinoma (HCC) after curative resection remain unknown. To investigate the prognostic value and non-invasive predictors of splenomegaly in ...

First reports of indigenous lethal infection with Anaplasma marginale, Anaplasma bovis ...
https://doi.org/10.1016/j.ttbdis.2020.101469
Ticks and Tick-borne Diseases; Jurković D, Mihaljević Ž et. al.

Jul 29th, 2020 - Anaplasmosis and theileriosis are important diseases with great economic impact that affect the cattle industry worldwide. In this study, we describe the first molecularly confirmed clinical cases of anaplasmosis caused by Anaplasma marginale and ...

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Guidelines  1 results

Revised diagnostic criteria and classification for the autoimmune lymphoproliferative s...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953894
Blood Oliveira JB, Bleesing JJ et. al.

Jun 11th, 2010 - Lymphadenopathy in children for which no infectious or malignant cause can be ascertained constitutes a challenging diagnostic dilemma. Autoimmune lymphoproliferative syndrome (ALPS) is a human genetic disorder of lymphocyte apoptosis resulting in...

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Drugs  1 results see all →

Clinicaltrials.gov  2,985 results

A wandering spleen, splenomegaly, hypersplenism, and iron deficiency anaemia.
https://doi.org/10.1016/S0140-6736(20)31552-X
Lancet (London, England); Pouchot J, Couprie A

Aug 10th, 2020 - A wandering spleen, splenomegaly, hypersplenism, and iron deficiency anaemia.|2020|Pouchot J,Couprie A,|

A mutation in NOTCH2 gene first associated with Hajdu-Cheney syndrome in a Greek family...
https://doi.org/10.1007/s12020-020-02446-7
Endocrine Efstathiadou ZA, Kostoulas C et. al.

Aug 8th, 2020 - Hajdu-Cheney Syndrome (HCS) is a rare genetic autosomal dominant disorder, characterized by distinctive facial features, acroosteolysis, and severe osteoporosis. Very rarely HCS is associated with polycystic kidney disease, splenomegaly or Crohn's...

Bone lesions in hairy cell leukemia: Diagnosis and treatment.
https://doi.org/10.1111/ejh.13505
European Journal of Haematology; Robak P, Jesionek-Kupnicka D et. al.

Aug 4th, 2020 - Skeletal involvement is a rare complication of hairy cell leukemia (HCL) with an incidence of approximately 3%. Bone lesions are commonly lytic and the most common sites of involvement are the femoral head and neck. Skeletal involvement is typical...

The prognostic value and non-invasive predictors of splenomegaly in cirrhotic patients ...
https://doi.org/10.17219/acem/81935
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University; Zhou L, Wang SB et. al.

Aug 3rd, 2020 - The prognostic value and non-invasive predictors of splenomegaly in cirrhotic patients with hepatocellular carcinoma (HCC) after curative resection remain unknown. To investigate the prognostic value and non-invasive predictors of splenomegaly in ...

First reports of indigenous lethal infection with Anaplasma marginale, Anaplasma bovis ...
https://doi.org/10.1016/j.ttbdis.2020.101469
Ticks and Tick-borne Diseases; Jurković D, Mihaljević Ž et. al.

Jul 29th, 2020 - Anaplasmosis and theileriosis are important diseases with great economic impact that affect the cattle industry worldwide. In this study, we describe the first molecularly confirmed clinical cases of anaplasmosis caused by Anaplasma marginale and ...

see more →

News  43 results

Atraumatic splenic rupture in acute myeloid leukemia
https://www.mdedge.com/ccjm/article/211092/hematology/atraumatic-splenic-rupture-acute-myeloid-leukemia?channel=263
Karthik Gnanapandithan, MD, MS

Nov 1st, 2019 - A 50-year-old man with acute myeloid leukemia (AML) with a complex karyotype was admitted to the hospital with several days of dull, left-sided abdominal pain. His most recent bone marrow biopsy showed 30% blasts, and immunophenotyping was suggest.

Long-acting interferon recommended for PV
https://www.mdedge.com/hematology-oncology/article/192212/cythemias/long-acting-interferon-recommended-pv
HT Staff

Dec 20th, 2018 - Image courtesy of AFIP Polycythemia vera The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has recommended approval for ropeginterferon alfa-2b (BESREMi®) to treat adults who have polycythemia vera (PV) without.

Adult-Onset Still Disease: Persistent Pruritic Papular Rash With Unique Histopathologic Findings
https://www.mdedge.com/dermatology/article/175877/rare-diseases/adult-onset-still-disease-persistent-pruritic-papular-rash/page/0/1

Sep 27th, 2018 - Comment Adult-onset Still disease is a systemic inflammatory condition that clinically manifests as spiking fevers, arthralgia, salmon-pink evanescent erythema, and lymphadenopathy. 2 The condition also can cause liver dysfunction, splenomegaly, pe.

A Case of Systemic Mastocytosis With Associated Clonal Hematological Non-Mast Cell Lineage Disease at VA Pittsburgh Healthcare System
https://www.mdedge.com/fedprac/avaho/article/174895/lymphoma-plasma-cell-disorders/case-systemic-mastocytosis-associated
Liman AD, Gandhi A et. al.

Sep 14th, 2018 - Introduction: Systemic mastocytosis (SM) is a rare myeloid neoplasm that is caused by accumulation of abnormal mast cells in the bone marrow, liver, spleen, and skin. The KIT D816V mutation encodes a constitutively activated receptor tyrosine kina.

Polycythemia Vera and Essential Thrombocythemia: Current Management
https://www.mdedge.com/hematology-oncology/article/156481/leukemia-myelodysplasia-transplantation/polycythemia-vera-and/page/0/4

Feb 6th, 2018 - Approach to Patients Refractory to or Intolerant of First-Line Therapy According to the European LeukemiaNet recommendations, an inadequate response to hydroxyurea in patients with PV (or myelofibrosis) is defined as a need for phlebotomy to maint.

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Patient Education  3 results see all →