The symptoms of Cushing disease are unmistakable to those who suffer from it – excessive weight gain, acne, distinct colored stretch marks on the abdomen, thighs and armpits, and a lump, or fat deposit, on the back of the neck. Yet the disorder often goes misdiagnosed.
To help combat misdiagnosis, Saleh Aldasouqi, an associate professor in the College of Human Medicine at Michigan State University, is drawing more attention to the rare disease through a case study, which followed a young patient displaying classic, yet more pronounced signs of the condition.
Saleh Aldasouqi is an associate professor and senior endocrinologist in the College of Human Medicine at Michigan State University. Courtesy photo
Caused mostly by small benign tumors in the pituitary gland that increase levels of the hormone cortisol, the disease and the growths initially can go undetected. Many of the symptoms are shared with other health issues, so the disease itself can be mistaken for obesity or depression in its early stages.
Aldasouqi, who is also a senior endocrinologist at the university, presented the study with MSU postgraduate students and co-authors Tiffany Burns, Deepthi Rao and Mamata Ojha, at the Endocrine Society’s annual International Congress of Endocrinology in Chicago on June 21.
For Sydney Kandell, her symptoms brought her to the emergency room multiple times over the course of a year with no clear diagnosis coming until she turned 18 years old. Now a community college student with aspirations of attending MSU in pediatric endocrinology, Kandell’s condition has greatly improved after treatment.
“What was so different about Sydney’s case was the size of the tumor we found and the excessive weight she put on in such a short amount of time,” Aldasouqi said.
“She gained about 100 pounds just in her senior year of high school, and her tumor was so much larger and more aggressive. It wreaked havoc on her body.” The aggressive tumor, known as Crooke’s Cell Adenoma, made Kandell’s case extremely rare with less than five percent, or about 100 cases like hers, reported worldwide.
The pea-size pituitary gland is part of the endocrine system and is found at the base of the brain. It’s often considered the master gland, controlling other glands such as the thyroid and adrenal, as well as many of the body’s everyday hormonal functions including body temperature, testosterone and estrogen.
“When you have even the smallest of tumors in this gland, it can significantly disrupt the way the body functions,” Aldasouqi said. “Sydney’s condition was elevated due to the size of her tumor, and now it’s through her story that other clinicians and even patients can learn to pay more attention to the symptoms and achieve an early diagnosis.”
Sarina Gleason | Eurek Alert!
Proteomics and precision medicine
08.02.2016 | University of Iowa Health Care
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Researchers at King’s College London and the Wellcome Trust Sanger Institute in the United Kingdom have for the first time demonstrated a direct link between the Wbp2 gene and progressive hearing loss. The scientists report that the loss of Wbp2 expression leads to progressive high-frequency hearing loss in mouse as well as in two clinical cases of children with deafness with no other obvious features. The results are published in EMBO Molecular Medicine.
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