Rufener E A
Br J Dermatol. 1987 May;116(5):703-8. doi: 10.1111/j.1365-2133.1987.tb05904.x.
Twelve people with erythropoietic protoporphyria (EPP) answered a written questionnaire and were subsequently interviewed. They had all learned to cope with the disease, but found their lives severely restricted. They found that they were seldom understood by others and they suffered considerable physical and psychological distress. Only one subject had any knowledge of the pathophysiological mechanism of EPP. The physician has an important role in recognizing this condition and in providing practical advice and supportive counselling to help patients cope with the disease.
12名红细胞生成性原卟啉病(EPP)患者填写了一份书面问卷,随后接受了访谈。他们都已学会应对这种疾病,但发现自己的生活受到严重限制。他们发现很少有人理解他们,并且遭受了相当大的身心痛苦。只有一名受试者了解EPP的病理生理机制。医生在识别这种疾病以及提供实用建议和支持性咨询以帮助患者应对疾病方面发挥着重要作用。