[The strange case of a patient affected by acromegaly with osteoporomalacia without hypogonadism].
نویسندگان
چکیده
Acromegaly is a rare disease that, in the majority of cases, is due to the presence of a benign growth hormone (GH)-producing tumor of the pituitary. Growth hormone has profound effects on linear bone growth, bone metabolism, and bone mass. In acromegaly, the skeletal effects of chronic GH excess have been mainly addressed by evaluating bone mineral density (BMD). Most data were obtained in patients with active acromegaly, and apparently high or normal BMD was observed in the absence of hypogonadism. The Autors describe a case of patient affected by acromegaly without hypogonadism with serious osteoporosis and biological signs of osteomalacia.
منابع مشابه
Unusual AIP mutation and phenocopy in the family of a young patient with acromegalic gigantism
Early-onset acromegaly causing gigantism is often associated with aryl-hydrocarbon-interacting receptor protein (AIP) mutation, especially if there is a positive family history. A15y male presented with tiredness and visual problems. He was 201 cm tall with a span of 217 cm. He had typical facial features of acromegaly, elevated IGF-1, secondary hypogonadism and a large macroadenoma. His patern...
متن کاملA rare challenging case of co-existent craniopharyngioma, acromegaly and squamous cell lung cancer
Co-existence of craniopharyngioma and acromegaly has been very rarely reported. A 65-year-old man presented with visual deterioration, fatigue and frontal headaches. Magnetic resonance imaging revealed a suprasellar heterogeneous, mainly cystic, 1.9 × 2 × 1.9 cm mass compressing the optic chiasm and expanding to the third ventricle; the findings were consistent with a craniopharyngioma. Pituita...
متن کاملStudy of cases of suicide with plaster as a new and strange way of suicide in Lorestan Province
Introduction: Suicide with plaster is a new and strange way of suicide which has been only committed in Lorestan province and its vicincy out skirts which have been occurred in recent years. Concerning the points of unclear border of this issue charactristics of victims patient's sign and symptoms, management, suitablecuring way, a study case has been done. Materials & Methods: This study co...
متن کاملA young girl with H syndrome and coeliac disease
H syndrome is an autosomal recessive genodermatosis with reports dating back to the last decade. This syndrome is caused by mutations in the SCL29A3 gene. The clinical characteristics of this syndrome consist of dermatological manifestations, including hyperpigmented, hypertrichotic, and indurated patches and plaques. It affects various systems by causing heart anomalies, hepatosplenomegaly, hy...
متن کاملMetastatic pituitary carcinoma in a patient with acromegaly: a case report
INTRODUCTION Asymptomatic pituitary abnormalities occur in about 10% of cranial magnetic resonance imaging scans, but metastatic carcinoma of the pituitary gland is rare: 133 cases have been reported. Two thirds secreted either prolactin or adrenocorticotropic hormone, and another 24% were non-secreting. CASE PRESENTATION A 42-year-old Caucasian man lived for 30 years after the diagnosis of a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Reumatismo
دوره 57 4 شماره
صفحات -
تاریخ انتشار 2005