出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2017/04/20 07:57:53」(JST)
Bleeding diathesis | |
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Classification and external resources | |
Specialty | hematology |
ICD-10 | D69.9 |
ICD-9-CM | 287.9 |
DiseasesDB | 1442 |
MeSH | D006474 |
[edit on Wikidata]
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In medicine (hematology), bleeding diathesis (h(a)emorrhagic diathesis) is an unusual susceptibility to bleed (hemorrhage) mostly due to hypocoagulability, in turn caused by a coagulopathy (a defect in the system of coagulation). Several types are distinguished, ranging from mild to lethal. Also, bleeding diathesis can be caused by thinning of the skin or impaired wound healing.[1]
Symptom | Disorders |
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Petechiae (red spots) |
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Purpura and ecchymoses |
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Blood in stool |
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Bleeding gingiva (gums) |
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Prolonged nose bleeds |
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While there are several possible causes, they generally result in excessive bleeding and a lack of clotting.
Acquired causes of coagulopathy include anticoagulation with warfarin, liver failure, Vitamin K deficiency and disseminated intravascular coagulation.Additionally, the haemotoxic venom from certain species of snakes can cause this condition, for example Bothrops, rattlesnakes and other species of viper. Viral hemorrhagic fevers include dengue hemorrhagic fever and Dengue Shock Syndrome
Leukemia may also cause coagulopathy. Furthermore, cystic fibrosis has been known to cause bleeding diathesis, especially in undiagnosed infants, due to malabsorption of fat soluble vitamins like Vitamin K.
There are autoimmune causes of coagulation disorders. They include acquired antibodies to coagulation factors, termed inhibitors of coagulation. The main inhibitor is directed against clotting Factor VIII. Another example is antiphospholipid syndrome an autoimmune, hypercoagulable state.
Bleeding diathesis may also be caused by impaired wound healing (as in scurvy), or by thinning of the skin, such as in Cushing's syndrome .
Some people lack genes that typically produce the protein coagulation factors that allow normal clotting. Various types of Hemophilia and von Willebrand disease are the major genetic disorders associated with coagulopathy.Rare examples are Bernard-Soulier syndrome, Wiskott-Aldrich syndrome and Glanzmann's thrombasthenia.
This section is empty. You can help by adding to it. (June 2016) |
Condition | Prothrombin time | Partial thromboplastin time | Bleeding time | Platelet count |
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Vitamin K deficiency or warfarin | Prolonged | Normal or mildly prolonged | Unaffected | Unaffected |
Disseminated intravascular coagulation | Prolonged | Prolonged | Prolonged | Decreased |
Von Willebrand disease | Unaffected | Prolonged or unaffected | Prolonged | Unaffected |
Haemophilia | Unaffected | Prolonged | Unaffected | Unaffected |
Aspirin | Unaffected | Unaffected | Prolonged | Unaffected |
Thrombocytopenia | Unaffected | Unaffected | Prolonged | Decreased |
Liver failure, early | Prolonged | Unaffected | Unaffected | Unaffected |
Liver failure, end-stage | Prolonged | Prolonged | Prolonged | Decreased |
Uremia | Unaffected | Unaffected | Prolonged | Unaffected |
Congenital afibrinogenemia | Prolonged | Prolonged | Prolonged | Unaffected |
Factor V deficiency | Prolonged | Prolonged | Unaffected | Unaffected |
Factor X deficiency as seen in amyloid purpura | Prolonged | Prolonged | Unaffected | Unaffected |
Glanzmann's thrombasthenia | Unaffected | Unaffected | Prolonged | Unaffected |
Bernard-Soulier syndrome | Unaffected | Unaffected | Prolonged | Decreased or unaffected |
Factor XII deficiency | Unaffected | Prolonged | Unaffected | Unaffected |
C1INH deficiency | Unaffected | Shortened | Unaffected | Unaffected |
This section is empty. You can help by adding to it. (June 2016) |
Following are some complications of coagulopathies, some of them caused by their treatments:
Complication | Disorders |
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Soft tissue bleeding, e.g. deep-muscle bleeding, leading to swelling, numbness or pain of a limb. |
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Joint damage, potentially with severe pain and even destruction of the joint and development of arthritis |
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Retinal bleeding |
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Transfusion transmitted infection, from blood transfusions that are given as treatment. |
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Adverse reactions to clotting factor treatment. |
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Anemia |
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Exsanguination (bleeding to death) |
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Cerebral hemorrhage |
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Diseases of clotting (D50–69,74, 280–287)
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Coagulation/ coagulopathy |
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リンク元 | 「出血傾向」「haemorrhagic diathesis」「出血性素因」 |
拡張検索 | 「albinism-hemorrhagic diathesis syndrome」 |
関連記事 | 「diathesis」「hemorrhagic」 |
血小板・ 血管壁 の異常 |
凝固異常 | 線溶異常 | |
出血部位 | 体表部(皮膚・粘膜) | 深部(皮下・筋肉・関節) | 深部組織に多い |
出血徴候 | 点状出血・小斑状出血 | 大斑状出血・後出血 | 後出血・漏出性出血 |
特徴 | 小さな傷でも出血するが圧迫で容易に止血しやすい | じわじわ出血がすすみ、局所止血で止まりにくい | 一旦出血が止まった後に再出血する |
出血症状 | 血小板、血管壁の異常 | 凝固因子の異常 |
点状出血 | 誘発する | 少ない |
粘膜出血 | 誘因なしに見られる | 機械的刺激、外傷の後に見られることが多い |
筋肉・関節内出血 | 基本的になし | 特徴的 |
外傷、手術後の出血 | 直後から見られる | しばらくたってから見られる。 |
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