Not functioning adrenocortical carcinoma from diagnosis to management: a case report

Authors

  • Bazrafshan, Behnaz Medical Cellular and Molecular Research Center, Golestan University of Medical Sciences, Gorgan, Iran
  • Fazel, Abdolreza Department of Surgery, 5-Azar Teaching Hospital, Golestan University of Medical Sciences, Gorgan, Iran
  • Hashempour, Mohammad Reza Students Research Committee, Department of Surgery, 5-Azar Teaching Hospital, Golestan University of Medical Sciences, Gorgan, Iran
  • Jouybari, Leila Nursing Research Center, Department of Nursing, Golestan University of Medical Sciences, Gorgan, Iran
  • Rostami, Masoomeh Department of Parasitology and Mycology, School of Medicine, Golestan University of Medical Sciences, Gorgan, Iran
  • Sanagoo, Akram Nursing Research Center, Department of Nursing, Golestan University of Medical Sciences, Gorgan, Iran
  • Sarmadi, Payam Family Medicine Department, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  • Shirangi, Seyed Payam Medical Cellular and Molecular Research Center, Golestan University of Medical Sciences, Gorgan, Iran
Abstract:

Abstract Adrenal gland cysts are rare indications of adrenal diseases, which are commonly asymptomatic. In radiological studies, these cysts, known as incidentalomas, are often detected by coincidence accounting for 6% of the population. Adrenal incidentalomas are commonly detected, and autonomous cortisol hypersecretion is the most prevalent abnormality associated with these masses. Since this complication is recurrent, it requires intermittent morphological and hormonal evaluation for several years. In this paper, we aimed to present the case of a 52-year-old woman with complaints of vague abdominal pain. After laparotomy, the tumor was removed, and umbilical herniorrhaphy was performed on the patient. Laparoscopic adrenalectomy is the first-line surgical treatment for this type of incidentaloma. Ultrasonography revealed an echogenic mass (diameter: 4 cm) in the left adrenal gland of the patient, which was not associated with hernia. In addition, CT-scan showed that the adrenal lesion was hypodense and heterogeneous (diameters: 81*53 mm) with sharp, irregular borders.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

not functioning adrenocortical carcinoma from diagnosis to management: a case report

abstract adrenal gland cysts are rare indications of adrenal diseases, which are commonly asymptomatic. in radiological studies, these cysts, known as incidentalomas, are often detected by coincidence accounting for 6% of the population. adrenal incidentalomas are commonly detected, and autonomous cortisol hypersecretion is the most prevalent abnormality associated with these masses. since this...

full text

[Disseminated adrenocortical carcinoma: case report].

Adrenocortical carcinoma is a rare neoplasm occurring with a frequency of 1-2 cases per million. It is characterized by significant malignancy with mean survival of about 28 months, and in the presence of documented metastases survival is shorter up to 8 months. This type of a tumor is slightly more frequent in women (58.6%) than in men (41.4%). Etiology of adrenocortical carcinoma is still unc...

full text

A case report of neonatal adrenocortical carcinoma

Results A boy was admitted to hospital at the age of 23 days because of vomiting, poor feeding and abdominal distension, and edema on both legs. On examination we found the child had Cushingoid syndrome, but not precocious puberty, edema on both legs, and hypertenstion. Blood pressure was 150/90 mmHg, required IV Loxen to maintain BP. Investigation showed cortisol 8AM was high of 4473 nmol/l; c...

full text

Adrenocortical carcinoma in a 8 years old child: a Case Report

Background:Unilateral tumors or masses of the adrenal gland are common. They are categorized as either functional (hormone-secreting) or silent and as either benign or malignant. Adrenocortical tumors are rare in childhood, with an incidence of 0.3-0.5 cases per one million child-years. Almost half of childhood tumors are adrenocortical carcinomas (ACC). Most ACCs are sporadic, but specialy i...

full text

Non functional adrenocortical carcinoma A case report

Adrenocortical carcinoma is a rare disease with an incidence of approximately 1-2 per million populations per year. The main symptoms are abdominal mass with or without endocrine dysfunction. However, there are difficulties in the diagnosis and treatment of this case due to its unspecific clinical presentation which sometimes require additional diagnostic methods such as immunohistochemistry. T...

full text

Adrenocortical Carcinoma Mimicking Pheochromocytoma: A case Report and Review of Literature

Adrenocortical carcinoma (ACC) is an uncommon malignancy originating from cortex of adrenal gland. The most common pitfall in diagnosis of ACC is to distinguish it from pheochromocytoma. Here we report a 62-year-old hypertensive man with presentation of dyspnea. The laboratory data showed an increase in urine cortisol and renin with a mild increase in aldosterone, but decrease in adrenocorticot...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 3  issue None

pages  56- 59

publication date 2016-12

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

No Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023