Results 41 to 50 of about 90,202 (191)
Introduction. Adrenal myelolipomas are uncommon nonfunctioning tumors of the adrenal. Synchronous renal cell carcinomas with adrenal myelolipomas are very rare.
Kallappan Senthil +4 more
doaj +1 more source
A Rare Mimicker of an Adrenal Carcinoma: Co-occurrence of Hemorrhagic Pseudocyst and Myelolipoma [PDF]
Adrenal collision tumors are rare tumors composed of two different benign or malignant tumors in the adrenal gland. Radiological features are very helpful in the diagnosis, however it is not always possible to make a definite diagnosis with imaging ...
Mesut Öztürk +6 more
core +1 more source
Abstract Objective To describe the procedure and short‐term outcomes of two dogs that underwent laparoscopic stapled partial cystectomy with intraoperative cystoscopy for excision of solitary, non‐trigonal, urothelial carcinoma lesions. Animals A 12‐year‐old female spayed mixed breed and a 13‐year‐old female spayed Siberian Husky.
Maureen A. Griffin +2 more
wiley +1 more source
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).
Alan Kelsall +4 more
wiley +1 more source
Adrenal Myelolipoma: A Case Report [PDF]
Adrenal myelolipoma is a rare benign tumor that is composed of hematopoietic cells and mature fat. Mostly, these nonfunctioning tumors are distinguished incidentally during autopsy or radiologic investigations.
Elham Jafari +3 more
doaj +1 more source
Myelolipoma of the adrenal gland
Abstract A case of myelolipoma in a 53-year-old man is presented (the fifth case of successful removal reported in the literature). The tumour was asymptomatic and was discovered during the investigation of painless haematuria. Selective angiography was found useful in the diagnosis, and associated malformations hinted at ...
D B, Tulcinsky, V, Deutsch, J J, Bubis
openaire +2 more sources
Congenital adrenal hyperplasia (CAH) due to 11β‐hydroxylase deficiency is an uncommon disorder characterized by impaired cortisol synthesis, hyperandrogenism, and mineralocorticoid excess. The coexistence of Leydig cell tumors (LCTs) and testicular adrenal rest tumors (TARTs) is rarely reported, highlighting the diagnostic and therapeutic challenges in
Shervin Mossavarali +4 more
wiley +1 more source
Laparoscopic excision of a giant adrenal myelolipoma and review of the literature
Introduction: Adrenal myelolipoma is a rare benign tumor. It is usually asymptomatic with variable sizes, where the small lesions are usually managed conservatively and the large and symptomatic ones indicate open or laparoscopic adrenalectomy ...
R.A. Gadelkareem +5 more
doaj +1 more source
Germ cell and other tumors in individuals with differences in sex development
Abstract Approximately one in 3500 to one in 5100 live‐born infants have atypical external genital development, known as differences in sex development (DSD). In 2005, an expert consensus conference thoroughly reviewed aspects of health care for individuals with DSD.
Selma Feldman Witchel +1 more
wiley +1 more source
Functioning adrenal adenomas are well-described entities that can rarely occur outside the adrenal gland in the ectopic adrenal tissue. Similarly, myelolipoma is an another benign lesion of the adrenal tissue which can rarely occur outside the adrenal ...
Lea F. Surrey +4 more
doaj +1 more source

