Essential Thrombocytosis: A Rare Entity
Essential thrombocytosis is a chronic myeloproliferative disorder of unknown etiology, which is characterized by persistent megakaryocytic proliferation, resulting in markedly increased platelets in circulation. We present the case of a 40-year-old female patient, who came with complaints of excessi...
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2023-01-01
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| Series: | Assam Journal of Internal Medicine |
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| Online Access: | https://journals.lww.com/10.4103/ajoim.ajoim_25_22 |
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| _version_ | 1849738133457862656 |
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| author | Parimi Ram Shashank Intikabur Rahman |
| author_facet | Parimi Ram Shashank Intikabur Rahman |
| author_sort | Parimi Ram Shashank |
| collection | DOAJ |
| description | Essential thrombocytosis is a chronic myeloproliferative disorder of unknown etiology, which is characterized by persistent megakaryocytic proliferation, resulting in markedly increased platelets in circulation. We present the case of a 40-year-old female patient, who came with complaints of excessive tiredness, infrequent tingling sensation at the tip of her fingers, and generalized body ache, and was initially detected to have extreme thrombocytosis of 1,775,000/mm3. On further evaluation, she was diagnosed with essential thrombocytosis and did not report any further deterioration throughout the follow-up period and is being maintained on low-dose aspirin. |
| format | Article |
| id | doaj-art-ae3bb0a9eca04de485fbbb1e37fedd15 |
| institution | DOAJ |
| issn | 2278-8239 |
| language | English |
| publishDate | 2023-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Assam Journal of Internal Medicine |
| spelling | doaj-art-ae3bb0a9eca04de485fbbb1e37fedd152025-08-20T03:06:43ZengWolters Kluwer Medknow PublicationsAssam Journal of Internal Medicine2278-82392023-01-01131363810.4103/ajoim.ajoim_25_22Essential Thrombocytosis: A Rare EntityParimi Ram ShashankIntikabur RahmanEssential thrombocytosis is a chronic myeloproliferative disorder of unknown etiology, which is characterized by persistent megakaryocytic proliferation, resulting in markedly increased platelets in circulation. We present the case of a 40-year-old female patient, who came with complaints of excessive tiredness, infrequent tingling sensation at the tip of her fingers, and generalized body ache, and was initially detected to have extreme thrombocytosis of 1,775,000/mm3. On further evaluation, she was diagnosed with essential thrombocytosis and did not report any further deterioration throughout the follow-up period and is being maintained on low-dose aspirin.https://journals.lww.com/10.4103/ajoim.ajoim_25_222022dibrugarhessential thrombocytosismyeloproliferative |
| spellingShingle | Parimi Ram Shashank Intikabur Rahman Essential Thrombocytosis: A Rare Entity Assam Journal of Internal Medicine 2022 dibrugarh essential thrombocytosis myeloproliferative |
| title | Essential Thrombocytosis: A Rare Entity |
| title_full | Essential Thrombocytosis: A Rare Entity |
| title_fullStr | Essential Thrombocytosis: A Rare Entity |
| title_full_unstemmed | Essential Thrombocytosis: A Rare Entity |
| title_short | Essential Thrombocytosis: A Rare Entity |
| title_sort | essential thrombocytosis a rare entity |
| topic | 2022 dibrugarh essential thrombocytosis myeloproliferative |
| url | https://journals.lww.com/10.4103/ajoim.ajoim_25_22 |
| work_keys_str_mv | AT parimiramshashank essentialthrombocytosisarareentity AT intikaburrahman essentialthrombocytosisarareentity |