Department of Clinical Hematology, King George's Medical University, Lucknow, Uttar Pradesh, India.
Department of Pathology, King George's Medical University, Lucknow, Uttar Pradesh, India.
Am J Case Rep. 2020 Jul 28;21:e924455. doi: 10.12659/AJCR.924455.
BACKGROUND Priapism is rarely reported as a complication in patients with essential thrombocythemia at presentation. We could find very few such cases of essential thrombocythemia while searching the literature. A combined modality of treatment is used in the form of chemotherapy and procedures like repeated aspiration and instillation of phenylephrine to treat essential thrombocythemia presenting with recurrent priapism. CASE REPORT A 31-year-old man presented to the Urology Department with priapism for the last 24 h. He had previously had multiple similar episodes in the last 20 days and 1 episode of prolonged penile erection 5 months ago. On examination, his penis was erect, swollen, and painful. There was no organomegaly. The priapism was managed with repeated aspiration and instillation of phenylephrine. Routine investigations showed marked thrombocytosis. Subsequent investigations done in the Clinical Hematology Department revealed increased megakaryocytes in bone marrow and presence of JAK2V617F mutation. After confirmation of diagnosis, cytoreductive therapy (hydroxyurea 500 mg twice a day) and acetyl salicylic acid 75 mg once a day was initiated. With this treatment, the platelet count normalized over a period of 2 months and no further episodes of priapism were noted; however, the patient developed erectile dysfunction. CONCLUSIONS Essential thrombocythemia can present with priapism as the first manifestation. Early suspicion, diagnosis, and management is needed to prevent erectile dysfunction. Erectile dysfunction is usually irreversible after long-standing priapism.
在初诊时,患有原发性血小板增多症的患者很少出现阴茎异常勃起的并发症。我们在文献检索中几乎找不到此类原发性血小板增多症病例。对于表现为反复性阴茎异常勃起的原发性血小板增多症,采用化疗和多次抽吸及苯肾上腺素灌注等联合治疗方法。
一名 31 岁男性因阴茎异常勃起 24 小时就诊于泌尿科。他在过去 20 天内有多次类似发作,5 个月前曾有 1 次长时间阴茎勃起。体格检查示阴茎勃起、肿胀、疼痛。无器官肿大。采用多次抽吸和苯肾上腺素灌注来处理阴茎异常勃起。常规检查显示明显的血小板增多。随后在临床血液科进行的检查显示骨髓中巨核细胞增多,并存在 JAK2V617F 突变。确诊后,开始进行细胞减少治疗(羟基脲 500mg,每日两次)和每天一次乙酰水杨酸 75mg。经过 2 个月的治疗,血小板计数恢复正常,且未再发生阴茎异常勃起,但患者出现了勃起功能障碍。
原发性血小板增多症可表现为阴茎异常勃起,为首发症状。早期诊断和治疗可预防勃起功能障碍。长期阴茎异常勃起后,勃起功能障碍通常不可逆转。