Cassol Clarissa A, Williams Michael P A, Caza Tiffany N, Rodriguez Sophia
Department of Pathology, The Ohio State University, Columbus.
Department of Pathology, SUNY Upstate Medical University, Oneida.
Medicine (Baltimore). 2019 Sep;98(39):e17148. doi: 10.1097/MD.0000000000017148.
Thrombotic microangiopathy (TMA) is a group of clinical syndromes characterized by excessive platelet activation and endothelial injury that leads to acute or chronic microvascular obliteration by intimal mucoid and fibrous thickening, with or without associated thrombi. It frequently involves the kidney but may involve any organ or system at variable frequencies depending on the underlying etiology. Among its numerous causes, drug toxicities and complement regulation abnormalities stand out as some of the most common. A more recently described association is with monoclonal gammopathy. Lung involvement by TMA is infrequent, but has been described in Cobalamin C deficiency and post stem-cell transplantation TMA.
This is the case of a patient with smoldering myeloma who received proteasome-inhibitor therapy due to retinopathy and developed acute renal failure within one week of therapy initiation.
A renal biopsy showed thrombotic microangiopathy. At the time, mild pulmonary hypertension was also noted and presumed to be idiopathic.
Given the known association of proteasome-inhibitor therapy with thrombotic microangiopathy, Bortezomib was discontinued and dialysis was initiated.
Drug withdrawal failed to prevent disease progression and development of end-stage renal disease, as well as severe pulmonary hypertension that eventually lead to the patient's death.
To our knowledge, this is the first reported case of pulmonary involvement by TMA associated with monoclonal gammopathy which appears to have been triggered by proteasome-inhibitor therapy. Clinicians should be aware of this possibility to allow for more prompt recognition of pulmonary hypertension as a potential manifestation of monoclonal gammopathy-associated TMA, especially in patients also receiving proteasome-inhibitors, so that treatment aiming to slow disease progression can be instituted.
血栓性微血管病(TMA)是一组临床综合征,其特征为血小板过度活化和内皮损伤,导致内膜黏液样和纤维性增厚,进而引起急性或慢性微血管闭塞,可伴有或不伴有血栓形成。它常累及肾脏,但根据潜在病因的不同,也可能以不同频率累及任何器官或系统。在其众多病因中,药物毒性和补体调节异常是一些最常见的原因。最近描述的一种关联是与单克隆丙种球蛋白病有关。TMA累及肺部并不常见,但在钴胺素C缺乏症和干细胞移植后TMA中已有报道。
本文报道了一例冒烟型骨髓瘤患者,因视网膜病变接受蛋白酶体抑制剂治疗,在治疗开始后一周内出现急性肾衰竭。
肾活检显示为血栓性微血管病。当时还发现轻度肺动脉高压,推测为特发性。
鉴于已知蛋白酶体抑制剂治疗与血栓性微血管病有关,停用硼替佐米并开始透析。
停药未能阻止疾病进展和终末期肾病的发展,以及严重肺动脉高压的发生,最终导致患者死亡。
据我们所知,这是首例报道的与单克隆丙种球蛋白病相关的TMA累及肺部的病例,似乎是由蛋白酶体抑制剂治疗引发的。临床医生应意识到这种可能性,以便更迅速地识别肺动脉高压是单克隆丙种球蛋白病相关TMA的潜在表现,尤其是在同时接受蛋白酶体抑制剂治疗的患者中,从而能够采取旨在减缓疾病进展的治疗措施。