Lang B, Meske S, Billmann P, Vaith P, Peter H H
Z Rheumatol. 1986 Mar-Apr;45(2):64-7.
In a twenty-nine year old female patient with progressive systemic sclerosis (scleroderma) (PSS) and an impressing involvement of the intestine (disturbance of the oesophageal motility, pseudo-obstruction, malabsorption) a spontaneous, asymptomatic pneumoperitoneum is observed. Perforation or pneumatosis cystoides intestinalis (PCI) could not be proved. The possible pathogenesis, course, prognosis and therapy of this rare complication are discussed.
在一名29岁患有进行性系统性硬化症(硬皮病)(PSS)且肠道受累明显(食管动力障碍、假性肠梗阻、吸收不良)的女性患者中,观察到自发性无症状气腹。未证实存在穿孔或肠壁囊样积气(PCI)。讨论了这种罕见并发症的可能发病机制、病程、预后及治疗。