scholarly journals Bleeding angiomyolipoma mimiking a ruptured adrenal tumour

2020 ◽  
Vol 28 ◽  
pp. 101031
Author(s):  
R.B. Nerli ◽  
Shridhar C. Ghagane ◽  
Vishal Kadeli ◽  
Shreeharsha Nutalpati ◽  
Sham Mohan ◽  
...  
Keyword(s):  
Adrenal Tumour

Functional adrenal tumour as a cause of virilised infant

2014 ◽  
Author(s):  
Rebecca Poole ◽  
Victoria Howard ◽  
Wendy Watts ◽  
Tafadzwa Makaya
Keyword(s):  
Adrenal Tumour

Differential diagnosis of adrenal tumour and upper pole renal tumour by I-131 cholesterol adrenocortical scintigraphy

1992 ◽  
Vol 24 (6) ◽  
pp. 597-601 ◽  
Author(s):  
M. Takeda ◽  
T. Torii ◽  
T. Nishiyama ◽  
Y. Katayama ◽  
T. Tsutsui ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Renal Tumour ◽  
Adrenal Tumour ◽  
Adrenocortical Scintigraphy

scholarly journals An oncocytic adrenal tumour in a patient with Birt-Hogg-Dubé syndrome

2013 ◽  
Vol 80 (6) ◽  
pp. 925-927 ◽  
Author(s):  
Victoria M. Raymond ◽  
Jessica M. Long ◽  
Jessica N. Everett ◽  
Elaine M. Caoili ◽  
Stephen B. Gruber ◽  
...  
Keyword(s):  
Adrenal Tumour

TUTANKHAMUN: AN ADRENAL TUMOUR ?

The Lancet ◽  
1972 ◽  
Vol 300 (7790) ◽  
pp. 1312 ◽  
Author(s):  
Malcolm Weller
Keyword(s):  
Adrenal Tumour

scholarly journals Adrenocortical Carcinoma in a 3 yrs Girl—A Case Report

1970 ◽  
Vol 22 (1) ◽  
pp. 142-143
Author(s):  
M Nowshad Ali ◽  
S Hoq Miah ◽  
M Meharunnesa ◽  
SM Badruddoza ◽  
Mushtaque Ahmed
Keyword(s):  
Case Report ◽  
Precocious Puberty ◽  
Cushing’S Syndrome ◽  
Adrenocortical Carcinoma ◽  
Pediatric Population ◽  
Signs And Symptoms ◽  
Cushing's Syndrome ◽  
Adrenal Tumour ◽  
Uncommon Tumour

Adrenocortical carcinoma is an uncommon tumour in the pediatric population. Account for only a small fraction of pediatric adrenal tumour. Most tumors in children are functional, and virilization is by far the most common presenting symptom, followed by Cushing's syndrome and precocious puberty. All patients with suspected adrenocortical carcinoma should be carefully evaluated for signs and symptoms of hormonal syndromes. DOI: 10.3329/taj.v22i1.5039 TAJ 2009; 22(1): 142-143

ADRENAL ANGIOMYOLIPOMA: A SURGICAL RARITY

2021 ◽  
pp. 22-23
Author(s):  
Mikail Merchant ◽  
Sushrut Tendulkar ◽  
Abhijit Thakur ◽  
Seelam Lakshmi Mounika
Keyword(s):  
Back Pain ◽  
Early Diagnosis ◽  
Adrenal Gland ◽  
Laparoscopic Resection ◽  
Accurate Diagnosis ◽  
Uneventful Recovery ◽  
Minimal Risk ◽  
Adrenal Tumour ◽  
Systemic Symptoms ◽  
Hormonal Assay

Adrenal Angiomyolipoma's are extremely rare forms of lipomatous tumours of adrenal gland. They may go undetected for years without symptoms. The patient may become symptomatic, once the tumour has gained a signicant size, mainly back pain. We are reporting our case which is a one of a kind benign Adrenal tumour. Adrenal Angiomylipomas are found as incidentalomas in patients, generally presenting with mild to no symptoms, leading to a long delay before they are diagnosed. However, early diagnosis is key, not only to alleviate symptoms but to also prevent a future surgical disaster due to rupture causing cardiovascular shock if large enough. Our patient presented with dull aching ank pain without any systemic symptoms. The diagnosis requires a multifocal approach to be conrmed including hormonal assay and radiological testing whereas following a “clinical only” approach maybe insufcient and often mislead a clinician from establishing an accurate diagnosis. These patients could be offered laparoscopic resection at specialized centres with minimal risk of complication and early uneventful recovery.

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