Alsalman Zaenb, Alsalman Mortadah, Albesher Mohammed, Alsalman Alaa, Saif Sultan, Aldandan Ali, Alsuliman Ahmed
Departments of Family Medicine, King Faisal University, Eastern Province, Saudi Arabia.
Departments of Medicine, King Faisal University, Eastern Province, Saudi Arabia.
Oxf Med Case Reports. 2022 May 23;2022(5):omac047. doi: 10.1093/omcr/omac047. eCollection 2022 May.
Primary myelofibrosis and paroxysmal nocturnal haemoglobinuria (PNH) are uncommon clonal blood disorders that are rarely found together. We report a case of primary myelofibrosis (PMF) with concomitant subtle PNH in a 42-year-old man who presented with a 4-week history of fatigue, unexplained chest pain, and new-onset erectile dysfunction. Bone marrow biopsy showed severe fibrosis consistent with PMF. However, smooth muscle dystonia symptoms in the form of new-onset erectile dysfunction and oesophageal spasm were not fully explained by PMF but were clues for PNH, confirmed by flow cytometric assays. Routine PNH testing for patients with new-onset PMF and clinical symptoms suggestive of PNH, as well as those with refractory anaemia despite effective therapy, is crucial since these two conditions can coexist. As a result, a lack of early testing may cause a delay in diagnosis, increasing the patient's transfusion load and the facility's costs.
原发性骨髓纤维化和阵发性夜间血红蛋白尿(PNH)是罕见的克隆性血液疾病,很少同时出现。我们报告一例42岁男性原发性骨髓纤维化(PMF)合并轻微PNH的病例,该患者有4周的疲劳、不明原因胸痛和新发勃起功能障碍病史。骨髓活检显示与PMF一致的严重纤维化。然而,新发勃起功能障碍和食管痉挛形式的平滑肌肌张力障碍症状不能完全用PMF解释,而是PNH的线索,流式细胞术检测证实了这一点。对新发PMF且有提示PNH临床症状的患者,以及尽管接受有效治疗仍有难治性贫血的患者进行常规PNH检测至关重要,因为这两种疾病可能共存。因此,缺乏早期检测可能导致诊断延迟,增加患者的输血负担和医疗机构的成本。