Wikipedia:
Grey platelet syndrome
Grey platelet syndrome (also spelled Gray platelet syndrome) is a rare condition caused by a reduction or
absence of the platelet alpha-granules in blood
platelets, or of the proteins contained in these granules.
See also
External links
- "The gray platelet syndrome: clinical spectrum of the disease.". Blood Rev. PMID
16442192.
|
Pathology: hematology
(primarily
C81-C96/200-208,
D45-D47, D50-D77/280-289) |
| WBCs |
hematological
malignancy (Lymphoma, leukemia)
-cytosis (Agranulocytosis, Leukocytosis,
Lymphocytosis, Monocytosis) • -penia
(Lymphopenia, Neutropenia) |
RBCs/anemia/
hemoglobinopathy |
nutritional anemia: Iron deficiency anemia, Plummer-Vinson syndrome,
Megaloblastic anemia (Pernicious
anemia)
hereditary hemolytic anemia: G6PD Deficiency, Thalassemia,
Sickle-cell disease/trait,
Hereditary spherocytosis, Hereditary elliptocytosis, Hereditary
stomatocytosis
acquired hemolytic anemia: Warm autoimmune hemolytic anemia,
HUS, MAHA,
PNH
aplastic anemia: Acquired
PRCA, Diamond-Blackfan anemia, Fanconi
anemia • Sideroblastic anemia • Hemochromatosis |
| Coagulation/platelets |
coagulopathy:
DIC • Hemophilia
(A, B, C,
XIII) • Von Willebrand
disease
Purpura: Henoch-Schönlein,
ITP, TTP
primary hypercoagulable state: Protein C deficiency - Protein S deficiency - Antithrombin III
deficiency
other hemorrhagic conditions: Bernard-Soulier syndrome -
Glanzmann's thrombasthenia - Grey platelet
syndrome |
| Histiocytosis |
WHO-I Langerhans cell histiocytosis - non-Langerhans-cell histiocytosis/WHO-II
(Juvenile xanthogranuloma, Hemophagocytic lymphohistiocytosis) - malignant histiocytic disorders/WHO-III
(Acute monocytic leukemia, Malignant
histiocytosis, Erdheim-Chester disease) |
| Other |
Asplenia/hyposplenism -
Methemoglobinemia |
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