A Child with Adrenocortical Adenoma Accompanied by Congenital Hemihypertrophy: Report of a Case

Surgery Today ◽  
2000 ◽  
Vol 30 (9) ◽  
pp. 861-865 ◽  
Author(s):  
Fujio Hara ◽  
Teruaki Kishikawa ◽  
Hirokazu Tomishige ◽  
Osamu Nishikawa ◽  
Yoshihisa Nishida ◽  
...  
Keyword(s):  
Adrenocortical Adenoma ◽  
Congenital Hemihypertrophy

MASSIVE ADRENOCORTICAL ADENOMA FOLLOWING LONG-TERM TREATMENT OF 21-HYDROXYLASE DEFICIENCY

2002 ◽  
Vol 167 (3) ◽  
pp. 1390-1391 ◽  
Author(s):  
SAYURI TAKAHASHI ◽  
SHIGERU MINOWADA ◽  
KYOUICHI TOMITA ◽  
NORIYUKI KATUMATA ◽  
TOSHIAKI TANAKA ◽  
...  
Keyword(s):  
Term Treatment ◽  
Adrenocortical Adenoma ◽  
Hydroxylase Deficiency ◽  
Long Term Treatment ◽  
21 Hydroxylase Deficiency

scholarly journals Radiomics: a new tool to differentiate adrenocortical adenoma from carcinoma

BJS Open ◽  
2021 ◽  
Vol 5 (1) ◽  
Author(s):  
F Torresan ◽  
F Crimì ◽  
F Ceccato ◽  
F Zavan ◽  
M Barbot ◽  
...  
Keyword(s):  
Machine Learning ◽  
Imaging Techniques ◽  
Second Order ◽  
Learning Approach ◽  
Adrenocortical Adenoma ◽  
Unsupervised Machine Learning ◽  
First Order ◽  
Main Challenge ◽  
Machine Learning Approach ◽  
Adrenocortical Tumours

Abstract Background The main challenge in the management of indeterminate incidentally discovered adrenal tumours is to differentiate benign from malignant lesions. In the absence of clear signs of invasion or metastases, imaging techniques do not always precisely define the nature of the mass. The present pilot study aimed to determine whether radiomics may predict malignancy in adrenocortical tumours. Methods CT images in unenhanced, arterial, and venous phases from 19 patients who had undergone resection of adrenocortical tumours and a cohort who had undergone surveillance for at least 5 years for incidentalomas were reviewed. A volume of interest was drawn for each lesion using dedicated software, and, for each phase, first-order (histogram) and second-order (grey-level colour matrix and run-length matrix) radiological features were extracted. Data were revised by an unsupervised machine learning approach using the K-means clustering technique. Results Of operated patients, nine had non-functional adenoma and 10 carcinoma. There were 11 patients in the surveillance group. Two first-order features in unenhanced CT and one in arterial CT, and 14 second-order parameters in unenhanced and venous CT and 10 second-order features in arterial CT, were able to differentiate adrenocortical carcinoma from adenoma (P < 0.050). After excluding two malignant outliers, the unsupervised machine learning approach correctly predicted malignancy in seven of eight adrenocortical carcinomas in all phases. Conclusion Radiomics with CT texture analysis was able to discriminate malignant from benign adrenocortical tumours, even by an unsupervised machine learning approach, in nearly all patients.

Congenital adrenocortical adenoma: case report and review of literature

2004 ◽  
Vol 34 (12) ◽  
pp. 991-994 ◽  
Author(s):  
Zahir U. Sarwar ◽  
Valerie L. Ward ◽  
David P. Mooney ◽  
Sylvia Testa ◽  
George A. Taylor
Keyword(s):  
Case Report ◽  
Adrenocortical Adenoma ◽  
Review Of Literature

Scintigraphic Features of a Pure Estrogen-Secreting Adrenocortical Adenoma in a Patient with Gynecomastia

2002 ◽  
Vol 27 (10) ◽  
pp. 741-742 ◽  
Author(s):  
FABIO MINUTOLI ◽  
GIORGIO RESTIFO PECORELLA ◽  
SEBASTIANO COSENTINO ◽  
RENATO LIPARI ◽  
SERGIO BALDARI
Keyword(s):  
Adrenocortical Adenoma

High [18F] 2-fluoro-2-deoxy-d-glucose (FDG) uptake of adrenocortical adenoma showing subclinical Cushing's syndrome

2003 ◽  
Vol 17 (5) ◽  
pp. 403-406 ◽  
Author(s):  
Akiko Shimizu ◽  
Noboru Oriuchi ◽  
Yoshito Tsushima ◽  
Tetsuya Higuchi ◽  
Jun Aoki ◽  
...  
Keyword(s):  
Cushing’S Syndrome ◽  
Cushing's Syndrome ◽  
Adrenocortical Adenoma ◽  
Subclinical Cushing’S Syndrome ◽  
Fdg Uptake

A exceptional collision tumor of primary adrenal angiosarcoma and non-functioning adrenocortical adenoma

2017 ◽  
Vol 213 (6) ◽  
pp. 702-705 ◽  
Author(s):  
Katsumi Takizawa ◽  
Kenichi Kohashi ◽  
Takahito Negishi ◽  
Kenichi Taguchi ◽  
Yuichi Yamada ◽  
...  
Keyword(s):  
Collision Tumor ◽  
Adrenocortical Adenoma

EPITHELIAL HEPATOBLASTOMA ASSOCIATED WITH CONGENITAL HEMIHYPERTROPHY AND CYSTATHIONINURIA: PRESENTATION OF A CASE

PEDIATRICS ◽  
1970 ◽  
Vol 46 (1) ◽  
pp. 66-73 ◽  
Author(s):  
C. F. Geiser ◽  
A. Baez ◽  
A. M. Schindler ◽  
V. E. Shih
Keyword(s):  
Amino Acid ◽  
Histological Study ◽  
The Body ◽  
Skin Fibroblasts ◽  
Congenital Hemihypertrophy ◽  
Urinary Amino

A 13-month-old boy with hepatoblastoma and hemihypertrophy is presented; this is the fifth known case with this association. Histological study showed that hemihypertrophy was related to cellular hyperplasia but not to hypertrophy of individual cells. Karyotypes of leukocytes and of skin fibroblasts from both sides of the body were normal. The association of hemihypertrophy and hepatoblastoma stresses the dysontogenetic origin of this neoplasm and signals the possibility of this tumor in children with asymmetry. Our patient showed cystathioninuria, which was related to the high content of cystathionine in his tumor. The presence of cystathioninuria in 7 of 10 patients with hepatoblastoma so far examined, shows the usefulness of urinary amino acid screening in the diagnosis of this rare childhood neoplasm.

SYNDROME OF CONGENITAL HEMIHYPERTROPHY, SHORTNESS OF STATURE, AND ELEVATED URINARY GONADOTROPINS

PEDIATRICS ◽  
1953 ◽  
Vol 12 (4) ◽  
pp. 368-376 ◽  
Author(s):  
HENRY K. SILVER ◽  
WILLIAM KIYASU ◽  
JACK GEORGE ◽  
WILLIAM C. DEAMER
Keyword(s):  
The Other ◽  
Congenital Hemihypertrophy

Two cases of a syndrome of hemihypertrophy, shortness of stature, and elevated levels of urinary gonadotropins are reported. One of the children was a male, the other a female. The hemihypertrophy and shortness of stature had been present since birth and the elevated gonadotropins were found at 5½ and 6 years, respectively. The possible relationship to other conditions in childhood including those which also have increased gonadotropins is discussed.

Pyoderma Gangrenosum Occurring in the Setting of Hypercortisolism Associated With Adrenocortical Adenoma: A Pathophysiological Paradox

2020 ◽  
Vol 20 (1) ◽  
pp. 95-97
Author(s):  
Chapman Wei ◽  
Elizabeth Hazuka ◽  
Peter DeRosa ◽  
Jill Paulson ◽  
Adam Friedman
Keyword(s):  
Pyoderma Gangrenosum ◽  
Adrenocortical Adenoma

Congenital hemihypertrophy with adrenal adenoma and medullary sponge kidney

1988 ◽  
Vol 61 (729) ◽  
pp. 851-853 ◽  
Author(s):  
Y. Tomooka ◽  
H. Onitsuka ◽  
T. Goya ◽  
Y. Hayashida ◽  
T. Kuroiwa ◽  
...  
Keyword(s):  
Adrenal Adenoma ◽  
Medullary Sponge Kidney ◽  
Congenital Hemihypertrophy
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