Hereditary spherocytosis

Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.

Leukemia

A cancer of the blood and bone marrow characterized by an abnormal proliferation of leukocytes.


Total: 5

                       


(per page)
PMID (PMCID)
28352784
(5329816)
 OTHER
A case report of hereditary spherocytosis with concomitant chronic myelocytic leukemia.
Xiaoqiu W, Bingmu F, Jinhong J, Zhigang Q, Guangli M, Yonghua L, Xiaoli W.
Open Med (Wars). 2016;11(1):152-154.
Hereditary spherocytosis (HS) and Chronic myelocytic leukemia (CML) are both life threatening hemotologic diseases.
28352784
(5329816)
 OTHER
A case report of hereditary spherocytosis with concomitant chronic myelocytic leukemia.
Xiaoqiu W, Bingmu F, Jinhong J, Zhigang Q, Guangli M, Yonghua L, Xiaoli W.
Open Med (Wars). 2016;11(1):152-154.
A case report of hereditary spherocytosis with concomitant chronic myelocytic leukemia.
22259634
(3259520)
 OTHER
Splenic infarction in a patient with autoimmune hemolytic anemia and protein C deficiency.
Park MY, Kim JA, Yi SY, Chang SH, Um TH, Lee HR.
Korean J Hematol. 2011;46(4):274-8.
Protein C deficiency with splenic infarction has been reported in patients with viral infection, hereditary spherocytosis, and leukemia.
22259634
(3259520)
 OTHER
Splenic infarction in a patient with autoimmune hemolytic anemia and protein C deficiency.
Park MY, Kim JA, Yi SY, Chang SH, Um TH, Lee HR.
Korean J Hematol. 2011;46(4):274-8.
Splenic infarction is most commonly caused by cardiovascular thromboembolism; however, splenic infarction can also occur in hematologic diseases, including sickle cell disease, hereditary spherocytosis, chronic myeloproliferative disease, leukemia, and lymphoma.
1616240
 FEMALE Infant
[Skin manifestations revealing monocytic leukemia. A case report].
Cuny JF, Truchetet F, Levy M, Cabut S, Hennequin JP, Grandidier M.
Ann Pediatr (Paris). 1992;39(4):261-3.
These skin lesions are not specific of leukemia and other diagnoses should be considered including histiocytosis, neuroblastoma, and skin erythropoiesis (in Torch syndrome, hemolytic disease of the newborn, hereditary spherocytosis, and twin-to-twin transfusion syndrome).