Results 61 to 70 of about 253,599 (183)
Pancreatic Neuroendocrine Tumor Leading to a Diagnosis of Multiple Endocrine Neoplasia Type 1
DEN Open, Volume 6, Issue 1, April 2026.ABSTRACT Pancreatic neuroendocrine neoplasms are rare but occasionally encountered. They are generally highly vascularized solid tumors, often round in shape with clear boundaries, defined contours, and a homogeneous internal structure. However, they can also present with atypical features, such as cystic degeneration, hemorrhage, calcification, and ...
Noriyuki Hirakawa +9 more
wiley +1 more source
Two cases synchronous atypical parathyroid adenomas and papillary thyroid carcinoma
Клиническая и экспериментальная тиреоидология, 2018 Most clinicians are well aware of the coexistence of medullary thyroid cancer and hyperparathyroidism in hereditary and sporadic multiple endocrine neoplasia syndromes.
Iya A. Voronkova +8 more
doaj +1 more source
Dermatologic Features of Endocrine Tumor Syndromes—Systematic Review and Meta‐Analysis
International Journal of Dermatology, Volume 65, Issue 3, Page 464-488, March 2026.ABSTRACT Endocrine tumor syndromes, including multiple endocrine neoplasia types 1, 2A, and 2B (MEN1, MEN2A, MEN2B), Carney complex (CNC), and PTEN hamartoma tumor syndrome (PHTS), are hereditary conditions characterized by multisystem tumor development.
Sára Pálla +8 more
wiley +1 more source
De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder
American Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 521-530, February 2026.ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil +8 more
wiley +1 more source
Acute Medicine &Surgery, Volume 13, Issue 1, January/December 2026.In severe acute pancreatitis, hypocalcemia is common and predicts severity. In this patient, serial corrected calcium monitoring showed an early rise from normal to above‐normal levels, prompting intact PTH measurement and diagnosis of primary hyperparathyroidism.
Mitsuki Yokota +6 more
wiley +1 more source
Case Reports in Hematology, Volume 2026, Issue 1, 2026.Introduction In young adults with severe hypercalcemia, both classically associated adult and pediatric causes must be considered. Here, we detail the report of a 21‐year‐old male whose case highlights an atypical presentation of severe hypercalcemia with predominant neuropsychiatric symptoms due to classical Hodgkin’s lymphoma.
Sana Kagalwalla +2 more
wiley +1 more source
Parathyroid Adenoma: is Sestamibi scintigraphy mandatory? [PDF]
, 2013 Localization of parathyroid adenoma using 99mTc scintigraphy is the standard of care. However, of late, ultrasound has been employed to this end with increasing frequency.1, 2, 3 The employment of intra-operative PTH estimation (IOPTH) has further ...
Vedachalam, Sucharitha; Madras Medical College +1 more
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Primary hyperparathyroidism presenting as acute hypercalcemic crisis: A case report
Journal of Otolaryngology - Head and Neck Surgery, 2023 Background Hyperparathyroid crisis, or “parathyroid storm” is a rare manifestation of primary hyperparathyroidism, characterized by sudden onset of symptomatic, severe hypercalcemia (> 3.5 mmol/L).
Gia Gill, Veena Agrawal, Paul Kerr
doaj +1 more source
Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.Parathyroid cancer (PC) is one of the rarest causes of primary hyperparathyroidism (PHPT), typically exhibiting an indolent course but presenting with more severe symptoms compared to its benign counterparts. The diagnosis is most often made postoperatively through histopathological examination; however, certain clinical and biochemical features may ...
Helena Fahmi +5 more
wiley +1 more source