Nadrous Hassan F, Krowka Michael J, McClure Rebecca F, Tefferi Ayalew, Lim Kaiser G
Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, Minnesota 55905, USA.
Leuk Lymphoma. 2004 Apr;45(4):815-8. doi: 10.1080/1042819032000141329.
Agnogenic myeloid metaplasia (AMM) is one of the myeloproliferative disorders, and is usually accompanied by extramedullary hematopoiesis (EMH) in various organs, mainly in the liver, spleen and lymph nodes. Extramedullary hematopoiesis and/or leukemic transformation of EMH in the pleura is a rare occurrence and is usually asymptomatic. Pleural involvement is usually diagnosed on postmortem examination. Herein we describe a 71-year-old man with newly diagnosed agnogenic myeloid metaplasia who was evaluated for progressively worsening dyspnea, pulmonary hypertension and bilateral pleural effusions. EMH involving the lungs and pleura was suspected. A sulfur colloid technetium 99m bone marrow scan performed to detect extramedullary hematopoiesis was negative. The diagnostic thoracentesis yielded bloody fluid that contained a large population of myeloblasts, indicating pleural leukemic transformation. The patient received 100 cGy to the whole lung for treatment of pulmonary hypertension due to EMH. This was followed by 1500 cGy total dose of radiation to the left lung for pleural extramedullary leukemic transformation. Pleural effusions resolved and repeat echocardiography showed reduction of the pulmonary artery pressure. Three months later he had leukemic transformation involving the skin and lymph nodes. Four months after radiation therapy, he had full-blown acute myeloid leukemia. He received 2 cycles of Gemtuzumab ozogamicin (Mylotarg), allopurinol and hydroxyurea. Three months after initiation of chemotherapy, he deteriorated and received salvage chemotherapy of prednisone, VP-16 and imatinib mesylate (Gleevec). He was hospitalized for neutropenic fever and was diagnosed to have pulmonary aspergillosis. He died of multisystem failure 8 1/2 months after being diagnosed with AMM.
原发性骨髓化生(AMM)是一种骨髓增殖性疾病,通常伴有髓外造血(EMH),累及多个器官,主要是肝脏、脾脏和淋巴结。胸膜的髓外造血和/或白血病转化较为罕见,通常无症状。胸膜受累通常在尸检时诊断。在此,我们描述一名71岁新诊断为原发性骨髓化生的男性,因进行性加重的呼吸困难、肺动脉高压和双侧胸腔积液接受评估。怀疑有累及肺部和胸膜的髓外造血。为检测髓外造血而进行的锝99m硫胶体骨髓扫描结果为阴性。诊断性胸腔穿刺抽出的血性液体中含有大量原始粒细胞,提示胸膜白血病转化。该患者因髓外造血导致的肺动脉高压接受了全肺100 cGy的照射。随后,对左肺进行了总量1500 cGy的放疗,以治疗胸膜髓外白血病转化。胸腔积液消退,重复超声心动图显示肺动脉压降低。三个月后,他出现了累及皮肤和淋巴结的白血病转化。放疗四个月后,他发展为急性髓系白血病。他接受了2个周期的吉妥珠单抗奥唑米星(Mylotarg)、别嘌醇和羟基脲治疗。化疗开始三个月后,他病情恶化,接受了泼尼松、依托泊苷(VP - 16)和甲磺酸伊马替尼(格列卫)的挽救性化疗。他因中性粒细胞减少性发热住院,被诊断为肺曲霉病。在被诊断为AMM 8个半月后,他死于多系统功能衰竭。