Raktapitta Nidana: Difference between revisions

Line 480:

===== II. Platelet abnormalities =====

#Thrombocytopenia: ① Diminished or defective platelet production: aplastic anemia, marrow infiltration (carcinoma, leukemia, myelofibrosis, tuberculosis, etc), infections, drugs that act on platelet production (alcohol, thiazide diuretics).② Enhanced platelet destruction: idiopathic thrombocytopenic purpura, drug-induced, thrombotic thrombocytopenic purpura. ~~③Sequestration~~ of platelets: hypersplenism

#Thrombocytopenia:

#Thrombocytosis: ① Primary: essential thrombocythemia.② Secondary: infections, injury, post-splenectomy chronic myelocytic leukemia, other myeloproliferative disorders (such as polycythemia vera)

##Diminished or defective platelet production: aplastic anemia, marrow infiltration (carcinoma, leukemia, myelofibrosis, tuberculosis, etc), infections, drugs that act on platelet production (alcohol, thiazide diuretics).

#Functional abnormalities of platelets: ① Congenital: thrombasthenia, giant platelet syndrome (Bernard-Soulier syndrome). ② Acquired: due to drugs, uremia, liver diseases, dysproteinemias

##Enhanced platelet destruction: idiopathic thrombocytopenic purpura, drug-induced, thrombotic thrombocytopenic purpura. ##Sequestration of platelets: hypersplenism

#Thrombocytosis:

##Primary: essential thrombocythemia.

##Secondary: infections, injury, post-splenectomy chronic myelocytic leukemia, other myeloproliferative disorders (such as polycythemia vera)

#Functional abnormalities of platelets:

##Congenital: thrombasthenia, giant platelet syndrome (Bernard-Soulier syndrome).

##Acquired: due to drugs, uremia, liver diseases, dysproteinemias

===== III. Coagulation disorders due to coagulation factor deficiencies =====

@@ Line 480: / Line 480: @@
 ===== II. Platelet abnormalities =====
-#Thrombocytopenia: ① Diminished or defective platelet production: aplastic anemia, marrow infiltration (carcinoma, leukemia, myelofibrosis, tuberculosis, etc), infections, drugs that act on platelet production (alcohol, thiazide diuretics).② Enhanced platelet destruction: idiopathic thrombocytopenic purpura, drug-induced, thrombotic thrombocytopenic purpura. ③Sequestration of platelets: hypersplenism
+#Thrombocytopenia:
-#Thrombocytosis: ① Primary: essential thrombocythemia.② Secondary: infections, injury, post-splenectomy chronic myelocytic leukemia, other myeloproliferative disorders (such as polycythemia vera)
+##Diminished or defective platelet production: aplastic anemia, marrow infiltration (carcinoma, leukemia, myelofibrosis, tuberculosis, etc), infections, drugs that act on platelet production (alcohol, thiazide diuretics).
-#Functional abnormalities of platelets: ① Congenital: thrombasthenia, giant platelet syndrome (Bernard-Soulier syndrome). ② Acquired: due to drugs, uremia, liver diseases, dysproteinemias
+##Enhanced platelet destruction: idiopathic thrombocytopenic purpura, drug-induced, thrombotic thrombocytopenic purpura. ##Sequestration of platelets: hypersplenism
+#Thrombocytosis:
+##Primary: essential thrombocythemia.
+##Secondary: infections, injury, post-splenectomy chronic myelocytic leukemia, other myeloproliferative disorders (such as polycythemia vera)
+#Functional abnormalities of platelets:
+##Congenital: thrombasthenia, giant platelet syndrome (Bernard-Soulier syndrome).
+##Acquired: due to drugs, uremia, liver diseases, dysproteinemias
 ===== III. Coagulation disorders due to coagulation factor deficiencies =====