Carcinoid tumour secreting dopa.

نویسندگان

  • B K Sharma
  • B J Smits
  • R Robinson
  • S Burns
  • E N Trounson
چکیده

A middle aged woman referred for an abdominal mass was found to have large amounts of dopa (3-4-dihydroxyphenylalanine) metabolites in her urine. At operation a tumour affecting almost the entire left lobe of the liver was removed. Histologically the tumour was a metastatic carcinoid. After operation the excretion of dopa metabolites fell substantially, confirming that the tumour was the source. Apparently, owing to an enzyme defect the tumour had been unable to decarboxylate dopa. These findings are further evidence of a neural origin for the endocrine system of the gut.

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

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

5-Hydroxyindole-secreting rectal carcinoid tumour.

A patient with a 5-hydroxyindole-secreting rectal carcinoid tumour is described, the second on record. There was no clinical evidence of carcinoid syndrome. Prostaglandin-like substances were isolated from hepatic metastases.

متن کامل

CASE REPORT Diagnosis and radioguided surgery with In-pentetreotide in a patient with paraneoplastic Cushing’s syndrome due to a bronchial carcinoid

In a 28-year-old man with Cushing’s syndrome, studies investigating a hypophyseal and/or adrenal origin of the disease, including computed tomography and magnetic resonance imaging, were negative. In agreement with reports showing somatostatin receptors on the cell membrane of ectopically secreting ACTH tumours, scintigraphy was performed after intravenous injection of 111 MBq Inpentetreotide (...

متن کامل

Cushing's syndrome and bronchial carcinoid tumour.

Adrenal function test results in a girl with Cushing's syndrome and a bronchial carcinoid tumour suggested pituitary dependent hypercortisolism. Resolution after excision of the tumour indicated that her condition had been caused by ectopic adrenocorticotrophic hormone secretion. Conventional tests of adrenal function may be misleading in cases of adrenocorticotrophic hormone secreting bronchia...

متن کامل

Carcinoid syndrome caused by a serotonin-secreting pituitary tumour.

BACKGROUND Neuroendocrine tumours are most frequently located in the gastrointestinal organ system or in the lungs, but they may occasionally be found in other organs. CASE We describe a 56-year-old woman suffering from a carcinoid syndrome caused by a large serotonin-secreting pituitary tumour. She had suffered for years from episodes of palpitations, dyspnoea and flushing. Cardiac disease h...

متن کامل

[Enteral nutrition for management of diabetic enteropathy: a case report].

several cases reported in the literature1,3,5--7 (in addition to our case) where 18FDG-PET (alone or combined with CT) was of value for the localization of occult ECS due to carcinoid tumor. Moreover, various studies have shown its value in detecting neuroendocrine tumors in general (secreting and non-secreting),8,9 mainly atypical ones (showing greater hypermetabolism).10 The development of ne...

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

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

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • British medical journal

دوره 288 6424  شماره 

صفحات  -

تاریخ انتشار 1984