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A Large Benign Adrenocortical Adenoma Cosecreting Testosterone and Cortisol
Martha Dillon and others
Most adrenal incidentalomas are benign neoplasms of the adrenal cortex. While the majority are nonfunctional, many secrete cortisol. Androgen- or estrogen-secreting adenomas are rare. A 44-year-old female, with history of hypertension and prediabetes, presented with worsening acne, hirsutism, ...
A Rare Prolactin-secreting Pituitary Carcinoma With Epidural and Thecal Metastases
Anna Liu and others
Pituitary carcinomas are rare but associated with significant morbidity and mortality. They remain challenging to diagnose and manage. In this case, we describe a 56-year-old man who presented with erectile dysfunction and binocular vertical diplopia. He had central hypogonadism, secondary adrenal ...
An Unexpected Case of Cutaneous Vasculitis Following Zoledronic Acid Infusion
Bita Zahedi and others
We report a case of isolated cutaneous small vessel vasculitis (SVV) occurring after zoledronic acid (Zol) infusion in a 58-year-old postmenopausal woman with a history of sleeve gastrectomy. This was the patient's first exposure to a bisphosphonate medication. Within minutes of the Zol infusion, ...
A Novel Variant in NR5A1 Presenting as 46,XY Difference of Sex Development
Yunting Yu and others
Differences of sex development (DSDs) are a spectrum of congenital clinical conditions involving the development of gonadal, chromosomal, and anatomical sex. The physical presentation provides incomplete clues because underlying etiologies may present with similar findings. We describe an ...
Giant Intracranial Meningiomas Requiring Surgery in 2 Transgender Women Treated With Cyproterone Acetate
Matthew I Balcerek and others
Progestin-associated meningioma is a rare complication of cyproterone acetate (CPA), an anti-androgen commonly prescribed in feminizing hormone therapy regimens for transgender and gender-diverse individuals. A dose-response association has been observed, particularly with longer-term exposure to ...
Multiple Primary Paragangliomas in a Pediatric Patient With von Hippel Lindau: A Diagnostic Dilemma
Katelin Magnan and others
Pheochromocytoma and paragangliomas (PPGLs) are rare chromaffin cell tumors arising from neural crest tissue. The majority of these tumors are nonmetastatic, with complete cure achieved through surgical resection. PPGLs have been associated with several hereditary cancer syndromes, including von ...
Correction to “Glucagon-like Peptide-1 Receptor Agonist Treatment With Semaglutide in Type 1 Diabetes”
In the above-named article by Raven LM, Greenfield JR, and Muir CA ( J Clin Endo Metab Case Reports . 2023; 1(1): 10.1210/jcemcr/luac017 ), a production error occurred in the PDF version of Figure 1 regarding patient information. The article has been corrected online. The publisher regrets the ...
Correction to: “Type B Insulin Resistance Syndrome: A Rare Cause of Hypoglycemia”
In the above-named article by Bhat SZ, Lim S, Sidhaye A, and Hamrahian AH ( JCEM Case Reports . 2023, 1(5); doi: 10.1210/jcemcr/luad104 ), there were errors throughout the article. In Table 2, the heading read: “Table 2. Clinical characteristics differentiating between type B insulin resistance ...
Rapidly Growing Thyroid Schwannoma: Diagnostic Challenges and Management Strategies
Freddy J K Toloza and others
Thyroid nodules are one of the most commonly encountered conditions in clinical endocrinology. Most thyroid nodules are of epithelial origin. However, primary thyroid mesenchymal tumors (TMTs), arising from the mesenchymal tissue, are being increasingly recognized. More than 20 different forms of ...
An Unusual Cause of Hypokalemia to Consider
Inés Borrego-Soriano and others
Apparent mineralocorticoid excess syndrome is a rare disorder that can be acquired through inhibition of the enzyme 11 β-hydroxysteroid dehydrogenase type 2 by various substances such as bile acids. We report the case of a 61-year-old woman presenting with painless jaundice. Computed tomography ...

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