Raised CA19.9 and hepatic space occupying lesion after teriparatide therapy in a case of polyostotic fibrous dysplasia

نویسندگان
چکیده

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A case of craniofacial polyostotic fibrous dysplasia.

We present the case of a patient with craniofacial polyostotic fibrous dysplasia. Polyostotic fibrous dysplasia is relatively rare and usually presents in late childhood/early adulthood. It is occasionally associated with endocrine disorders such as McCune-Albright syndrome. The benign pathology of this bone tumor belies its implications in the region of the skull base. Craniofacial polyostotic...

متن کامل

Polyostotic fibrous dysplasia; a case report.

Fibrous dysplasia is a condition leading to abnormal differentiation of osteoblasts which leads to replacement of normal bone with fibrous stroma [1-3]. It may involve single bone (monostotic) or multiple bones (polyostotic). It may affect any bone however; skull and ribs are the commonest [2,4-6]. It is usually asymptomatic and is an incidental finding. It may become symptomatic when complicat...

متن کامل

Bisphosphonate therapy in polyostotic fibrous dysplasia.

INDIAN PEDIATRICS 1069 VOLUME 41OCTOBER 17, 2004 attenuation of prostatic tissue seen in congenital obstructions leads to loss of obliquity of the normal ejaculatory ducts as they enter the posterior urethra. Associated distal obstruction to the flow of urine may aid in the urethro-ejaculatory reflux of urine .If the urine is infected, this precipitates epididymo-orchitis as it happened in the ...

متن کامل

Polyostotic fibrous dysplasia.

An 18-year-old man was referred to the authors' institution's thoracic cancer specialists for further consultation after abnormal findings were seen on chest radiograph.

متن کامل

Pathologic hepatic Tc-99m-MDP uptake in polyostotic fibrous dysplasia.

Fibrous dysplasia of bone is a congenital, sporadic developmental disorder characterized by immature fibrous connective tissue and bone deformities. Hepatic Tc-99m-MDP uptake is a rare, serendipitous finding during bone scanning studies. The present patient was a 25-year-old male who had severe polyostotic fibrous dysplasia. On Tc-99m-MDP (methylene diphosphonate) bone scintigraphy, increased a...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Indian Journal of Endocrinology and Metabolism

سال: 2013

ISSN: 2230-8210

DOI: 10.4103/2230-8210.117209