von Recklinghausen disease complicated by pulmonary hypertension.
نویسندگان
چکیده
Two patients with von Recklinghausen disease (neurofibromatosis type 1) were admitted to the hospital because of progressive heart failure. Both patients had prominent pulmonary hypertension revealed on cardiac catheterization. A lung perfusion scan did not show any gross defect. There were no underlying causes of pulmonary hypertension in either patient, such as chronic lung disease, congenital or acquired heart disease, deep vein thrombosis, or systemic hypercoagulable states. There may be an unrecognized association between von Recklinghausen disease and pulmonary hypertension.
منابع مشابه
گزارش یک مورد از هیپرتانسیون ترومبوآمبولیک پولمونر در جریان سندروم آنتی فسفولیپید اولیه
While pulmonary thromboembolism is common, thromboembolic pulmonary hypertension is very rare. The present case is a 35 year old woman with chronic thromboembolic pulmonary hypertension, who presented with severe dyspnea and leg edema, following an earlier thrombotic event of 10 years earlier, after her her second childbearing. She also had a history of the first childbearing complicated with c...
متن کاملبروز بدخیمی در ضایعات نوروفیبروماتوز در بیمار مبتلا به وون رکلین هاوزن
Neurofibromatosis (Von Recklinghausen syndrome) is an autosomal dominant genetic disease caused by a mutation in the gene expressing neurofibromin. It is characterized by café-au-lait macules, axillary or inguinal freckling, multiple neurofibromas, and developmental delay. Malignant transformation or sarcomatosis may occur in as many as 1.5-15% of patients. Case report: We present a patient wi...
متن کامل[Neurofibromatosis type 1 with interstitial pulmonary lesions diagnosed in adult patient. A case study and literature review].
A case of a 43-year-old man with clinically diagnosed neurofibromatosis type I (NF-1, von Recklinghausen disease), was referred to a lung disease unit in order to diagnosis of worsening tolerance to physical effort, and aetiology of radiological cystic lesions in the lungs, seen in the high-resolution computed tomography (HRCT). Since childhood the patient has been treated for epilepsy, and a ...
متن کاملExophtalmie pulsatile révélant une agénésie sphéno-orbitaire dans la maladie de Von-Recklinghausen
Les manifestations ophtalmologiques au cours de la maladie de Von Recklinghausen sont rares. Seulement quelques cas ont été rapportés dans la littérature internationale. Nous rapportons un cas d'exophtalmie pulsatile révélatrice d'une agénésie sphéno-orbitaire au cours de la maladie de Von Recklinghausen. which permits unrestricted use, distribution, and reproduction in any medium, provided the...
متن کاملNeurofibroma of the mandible in an adolescent with von Recklinghausen's disease.
Neurofibromatosis, as identified by yon Recklinghausen, is an autosomal dominant, neurocutaneous syndrome, characterized by multiple neurofibromas, cafe-au-lait spots, and iris Lisch nodules.1, 2 This disorder has also been referred to as the "Elephant Man" disease, and was the subject of a play and movie depicting the life of Joseph Merrick, who suffered severely from neurofibromatosis. 2 Othe...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Chest
دوره 119 5 شماره
صفحات -
تاریخ انتشار 2001