Results 31 to 40 of about 5,333 (238)

Adrenocortical Adenoma with Foci of Myelolipoma in a Patient of Conn’s Syndrome [PDF]

open access: yesNational Journal of Laboratory Medicine, 2017
Adrenal myelolipoma is an uncommon benign tumour usually discovered by chance in patients. It is usually inactive hormonally and composed of mature adipose tissue with normal haematopoietic cells.
Debosmita Bhattacharyya   +3 more
doaj   +1 more source

GIANT ADRENAL GANGLIONEUROMA AND MYELOLIPOMA: A RARE CASE OF COLLISION TUMOR.

open access: yesActa Endocrinologica, 2022
Background An adrenal collision tumor is a rare entity. We present a rare combination of giant adrenal ganglioneuroma (GN) and myelolipoma. GN is a rare benign tumor of the adrenal medulla that originates from primitive neural crest cells, while ...
P. Saraf   +3 more
semanticscholar   +1 more source

Presacral Myelolipoma [PDF]

open access: yes, 2014
Many reports have described adrenal myelolipomas but there have been only a few reports of extra-adrenal myelolipomas. We describe a 74-year-old woman who came to our observa- tion for MRI of the lumbar spine for typical lumbar back pain.
FALANGA, Giorgia   +6 more
core   +1 more source

Left-sided giant adrenal myelolipoma secreting catecholamine

open access: yesIndian Journal of Pathology and Microbiology, 2012
Adrenal myelolipoma (AML) is a rare benign tumor composed of mature adipose and hematopoietic tissue. Most of these patients are asymptomatic and the tumors are non-secreting.
Sujatha Udupa   +3 more
doaj   +1 more source

Benign Adrenal Adenomas Are Associated With Reduced Prevalence of Hospitalised Patients With COVID-19. [PDF]

open access: yesClin Endocrinol (Oxf)
ABSTRACT Introduction Adrenal incidentalomas (AI) are commonly found on imaging done for indications other than to assess the adrenal glands. Prevalence increases with age and is around 10% in people over 80 years. The majority of AIs are benign adenomas, with 20%−50% exhibiting mild autonomous cortisol secretion (MACS).
Kelsall A   +4 more
europepmc   +2 more sources

Mielolipoma adrenal gigante associado à deficiência da 21-hidroxilase: associação não usual simulando um carcinoma adrenocortical secretor de androgênios [PDF]

open access: yes, 2010
The objective of this study was to describe a case of giant myelolipoma associated with undiagnosed congenital adrenal hyperplasia (CAH) due to 21-hydroxylase (21OH) deficiency.
CASTRO, Margaret de   +6 more
core   +2 more sources

Intra-abdominal bleeding with hemorrhagic shock: a case of adrenal myelolipoma and review of literature

open access: yesBMC Surgery, 2017
Background Adrenal myelolipoma is an uncommon, benign, and hormonally non-functioning tumor that is composed of mature adipose tissue and normal hematopoietic tissue. Most cases to date are asymptomatic or have epigastric pain.
Hui-Pu Liu   +7 more
doaj   +1 more source

Adrenal lipomatous tumours: a 30 year clinicopathological experience at a single institution [PDF]

open access: yes, 2001
AIMS: Fatty tumours of the adrenal gland are uncommon and their features have received little attention in the literature. The aim of this study is to analyse the features of adrenal lipomatous tumours.
Lam, AKY, Lo, CY
core   +1 more source

Giant Adrenal Myelolipoma and Congenital Adrenal Hyperplasia: a Case Report and Review of the Literature

open access: yesSN Comprehensive Clinical Medicine, 2022
Introduction Adrenal myelolipomas (AMs) are rare, benign tumors without endocrine activity comprised of mature adipose and hematopoietic tissue. Surgical excision may be required for lesions which have associated symptoms, those that are growing, or have
Stephanie Y. Chen   +6 more
semanticscholar   +1 more source

Adrenal Myelolipoma: 369 Cases From a High-Volume Center

open access: yesFrontiers in Cardiovascular Medicine, 2021
Background: Adrenal myelolipoma (AML) is a nonfunctional benign neoplasm from the adrenal cortex, composed of mature fat and hematopoietic tissue. Usually, patients have no symptoms.
Lede Lin   +6 more
semanticscholar   +1 more source

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