Items tagged “adrenal gland”
22 results found
Article
Neuroblastoma
Neuroblastomas are tumours of neuroblastic origin. Although they may occur anywhere along the sympathetic chain, the vast majority arise from the adrenal gland.
They represent the most common extracranial solid childhood malignancy and are the third commonest childhood tumour after leukaemia an...
Case
Adrenal cortical carcinoma
Published
16 Aug 2009
65% complete
CT
Case
Adrenal myelolipoma
Published
16 Aug 2009
78% complete
CT
MRI
Article
Adrenal lesions (differential)
Adrenal lesions cover a broad spectrum from benign to neoplastic entities. Due to increased use of cross-sectional imaging they are frequently detected as incidental lesions (incidentalomas). If found incidentally, please refer to the Management of Incidental Adrenal Masses: American College of ...
Article
Neuroblastoma vs Wilms tumour
Both neuroblastoma and Wilms tumour occur in early childhood and typically present as large abdominal masses closely related to the kidneys. Distinguishing between the two is important, and a number of features are helpful.
Neuroblastoma
calcification very common: 90%
encases vascular st...
Article
Congenital neuroblastoma
Congenital neuroblastoma is defined as neuroblastoma identified within a month of birth, and is divided into:
fetal neuroblastoma
neonatal neuroblastoma
In most cases they present as stage 1, 2 or 4S (see neuroblastoma staging).
Fetal neuroblastoma
In 90% of cases, fetal neuroblastomas aris...
Article
Phaeochromocytoma
Phaeochromocytomas are an uncommon tumour of the adrenal gland, with characteristic clinical, and to a lesser degree, imaging features. The tumours are said to follow a 10% rule:
~10% are extra-adrenal
~10% are bilateral
~10% are malignant
~10% are found in children
~10% are not associated ...
Case
Neonatal neuroblastoma
Published
30 Apr 2010
74% complete
Ultrasound
CT
X-ray
Case
Adrenal adenoma
Published
28 Jun 2010
80% complete
CT
Article
Adrenal cortical carcinoma
An adrenal cortical carcinoma, also known as adrenocortical carcinoma, is a highly malignant but rare primary neoplasm of the adrenal gland. It may present as a hormonally active or inactive tumour.
Epidemiology
Although men and women are affected equally, functioning tumours are more common ...
Article
Adrenal gland tumours
Despite its small size, the adrenal gland is affected by a relatively large number of neoplastic entities:
adrenal adenoma
adrenal myelolipoma
adrenal cortical carcinoma
adrenal phaeochromocytoma
adrenal neuroblastoma
adrenal sarcoma
adrenal metastases
See also
adrenal lesions: for a mo...
Case
Phaeochromocytoma (gross pathology)
Published
25 Sep 2010
44% complete
Pathology
Article
Primary pigmented nodular adrenal dysplasia
Primary pigmented nodular adrenal dysplasia (PPNAD) is a rare benign adrenal condition characterised by ACTH-independent autonomous hypersecretion of cortisol, leading to Cushing syndrome.
Epidemiology
PPNAD is often familial. Patients typically present as children or young adults, and there ...
Case
Primary pigmented nodular adrenal dysplasia (gross pathology)
Published
29 Sep 2010
41% complete
Pathology
Case
Adrenal haemangioma
Published
11 Oct 2010
92% complete
CT
Article
Adrenal haemangioma
Adrenal haemangiomas are rare benign tumours that are usually incidentally identified (one example of an adrenal incidentaloma). Its significance mainly relates to the difficulty in differentiation from other malignant lesions.
Epidemiology
Although these can be found at any age, they are mos...
Case
Adrenocortical carcinoma
Published
20 Oct 2010
53% complete
MRI
Article
Adrenal gland
The adrenal (suprarenal) glands (often shortened to just the adrenals) are paired organs of the endocrine system, often asymmetric in shape.
Gross anatomy
The adrenal glands are located superior and anteromedial to the kidneys, within the perirenal space, and enclosed by perirenal fascia. Eac...
Case
Phaeochromocytoma (pathology)
Published
16 Apr 2013
79% complete
Pathology
Article
Congenital adrenal hyperplasia
Congenital adrenal hyperplasia, previously known as adrenogenital syndrome, is a group of seven autosomal recessive disorders relating to an enzyme deficiency affecting adrenal steroidogenesis.
Epidemiology
The incidence is highly variable depending on the enzyme deficiency, ranging from 1 in ...