Carvalhosa Ana B, Aouba Achille, Damaj Gandhi, Canioni Danielle, Brouzes Chantal, Gyan Emmanuel, Durupt Stéphane, Durieu Isabelle, Cathebras Pascal, Costédoat-Chalumeau Nathalie, Launay David, Pilmis Benoit, Barete Stephane, Frenzel Laurent, Lortholary Olivier, Hermine Olivier, Hermans Cedric, Chandesris Marie-Olivia
From the French Reference Centre for Mastocytosis (CEREMAST), Necker Children's Hospital, Assistance Publique - Hôpitaux de Paris (APHP), France (ABC, GD, DC, CB, SB, LF, OL, OH, M-OC); Haemostasis and Thrombosis Unit, Haemophilia Clinic, Division of Haematology, St-Luc University Hospital, Brussels, Belgium (ABC, CH); Department of Internal Medicine, Caen University Hospital, France (AA); Department of Haematology, Caen University Hospital, France (GD); Department of Pathology, Necker Children's Hospital, APHP, France (DC); Department of Biological Haematology, Necker Children's Hospital, APHP, France (CB); Department of Haematology and Cell Therapy, Tours University Hospital, France (EG); Department of Internal and Vascular Medicine, Lyon Sud University Hospital, France (SD, ID); Department of Internal Medicine, Saint-Etienne University Hospital, France (PC); Department of Internal Medicine, Cochin Hospital, APHP, France (NC-C); Department of Internal Medicine, Lille University Hospital, France (DL); Infectious Diseases Department, Necker Children's Hospital, APHP, France (BP, OL); Department of Dermatology, Tenon University Hospital, APHP, France (SB); Department of Haematology, Necker Children's Hospital, APHP, France (LF, OH, M-OC); and Sorbonne Paris Cité, Paris Descartes University, Imagine Institute, Paris, France (LF, OL, OH, M-OC).
Medicine (Baltimore). 2015 Oct;94(40):e1414. doi: 10.1097/MD.0000000000001414.
Mastocytosis is characterized by a clonal mast cell proliferation with organ infiltration and uncontrolled degranulation. Although not characteristic and poorly explained, some patients develop clotting abnormalities. We retrospectively identified patients with established diagnosis of mastocytosis and related clotting abnormalities (clinical and/or biological) using the national French Reference Centre for Mastocytosis database. From our cohort of 14 adult patients with clotting abnormalities (median age 46 years [range 26-75]), 4 had a presentation suggestive of a primary hemostasis disorder alone (by their symptoms and/or abnormal clotting tests [PFA, von Willebrand's disease [vWD] screening]) and 10 had a laboratory impairment of secondary hemostasis. Among these, 7 had bleeds characteristic of a coagulation cascade disorder (severe/life-threatening in 5 and mild in 2 patients). Clotting abnormalities were of variable severity, typically related to intense crisis of degranulation, such as anaphylactic reactions, and/or to severe organ infiltration by mast cells. Importantly, classical hemostatic management with platelet transfusion, fresh frozen plasma, or vitamin K infusions was unsuccessful, as opposed to the use of agents inhibiting mast cell activity, particularly steroids. This illustrates the crucial role of mast cell mediators such as tryptase and heparin, which interfere both with primary (mainly via inhibition of von Willebrand factor) and secondary hemostasis. There was interestingly an unusually high number of aggressive mastocytosis (particularly mast cell leukemia) and increased mortality in the group with secondary hemostasis disorders (n = 5, 36% of the whole cohort). Mast cell degranulation and/or high tumoral burden induce both specific biologic antiaggregant and anticoagulant states with a wide clinical spectrum ranging from asymptomatic to life-threatening bleeds. Hemostatic control is achieved by mast cell inhibitors such as steroids.
肥大细胞增多症的特征是克隆性肥大细胞增殖伴器官浸润和不受控制的脱颗粒。虽然不具有特征性且难以解释,但一些患者会出现凝血异常。我们使用法国国家肥大细胞增多症参考中心数据库,回顾性地确定了已确诊肥大细胞增多症及相关凝血异常(临床和/或生物学)的患者。在我们的14例有凝血异常的成年患者队列中(中位年龄46岁[范围26 - 75岁]),4例仅表现出提示原发性止血障碍(根据其症状和/或异常凝血试验[血小板功能分析仪检测、血管性血友病因子(vWD)筛查]),10例存在继发性止血的实验室损害。其中,7例有凝血级联障碍特征性的出血(5例严重/危及生命,2例轻度)。凝血异常的严重程度各不相同,通常与强烈的脱颗粒危机有关,如过敏反应,和/或与肥大细胞的严重器官浸润有关。重要的是,与使用抑制肥大细胞活性的药物(特别是类固醇)相反,采用血小板输注、新鲜冷冻血浆或维生素K输注的传统止血治疗未成功。这说明了肥大细胞介质如类胰蛋白酶和肝素的关键作用,它们干扰原发性止血(主要通过抑制血管性血友病因子)和继发性止血。有趣的是,在继发性止血障碍组(n = 5,占整个队列的36%)中,侵袭性肥大细胞增多症(特别是肥大细胞白血病)的数量异常高且死亡率增加。肥大细胞脱颗粒和/或高肿瘤负荷会导致特定的生物抗聚集和抗凝状态,临床谱范围从无症状到危及生命的出血。使用类固醇等肥大细胞抑制剂可实现止血控制。