Results 31 to 40 of about 4,980 (206)

Neuroendocrine tumours of the female genital tract: a case-based imaging review with pathological correlation [PDF]

, 2015
Background Both primary and secondary gynaecological neuroendocrine (NE) tumours are uncommon, and the literature is scarce concerning their imaging features.
Callé, Catarina, Cunha, Teresa Margarida, Dias, João Lopes, Félix, Ana, Gomes, Filipe Veloso   +4 more
core   +1 more source

Endocrine paraneoplastic syndromes in patients with neuroendocrine neoplasms [PDF]

Endocrine, 2018
Our aim was to assess the prevalence of endocrine paraneoplastic syndromes (EPNS) in neuroendocrine neoplasms (NENs) and estimate its impact on patient outcomes.This is a retrospective analysis of 834 patients with NENs (611 gastrointestinal, 166 thoracic, 57 of unknown and various other primary origin). We included 719 consecutive NEN patients treated
Kosmas Daskalakis, Eleftherios Chatzelis, Marina Tsoli, Nektaria Papadopoulou-Marketou, Georgios K. Dimitriadis, Apostolos V. Tsolakis, Gregory Kaltsas   +6 more
openaire   +6 more sources

Clinical challenges of paraneoplastic endocrine metabolic syndromes: An illustrative example

Journal of Clinical and Translational Endocrinology Case Reports
Background/objective: Paraneoplastic endocrine metabolic syndromes are rare, but clinically significant manifestations of underlying malignancies, often complicating clinical course and impacting treatment outcomes.
Srushti Shankar, Sumal S. Sundar, Madhumati S. Vaishnav, Leena Lekkala, Chandraprabha Siddalingappa, Kavitha Muniraj, Thummala Kamala, Reshma B. Vijay, Vasanthi Nath, Mandyam D. Chitra, Pushpa Ravikumar, Siddartha Dinesha, Tejeswini Deepak, Srikanta Sathyanarayana   +13 more
doaj   +1 more source

Coincidental Central Precocious Puberty and Wilms Tumor in a 5-Year-Old Girl

Case Reports in Pediatrics, 2019
Wilms tumor is the most frequent pediatric renal malignancy, and its usual presentation is an abdominal mass or hematuria. Unusual presentations have also been reported, such as paraneoplastic syndromes (acquired von Willebrand disease, sudden death due ...
Laura Kasongo, Patricia Forget, Ramona Corina Nicolescu   +2 more
doaj   +1 more source

Recurrent Hypothermia and Autonomic Dysfunction Secondary to Shapiro Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT A 44‐year‐old man presented with recurrent hypothermia, diaphoresis and hypertension. Extensive investigation for infectious, inflammatory, metabolic and endocrine aetiologies was negative. MR scan of the brain demonstrated no lesions but revealed callosal dysgenesis, consistent with Shapiro syndrome.
Naveen Kumar, Jeremy Johnson, Susanne Watkins, Eoin Mulroy   +3 more
wiley   +1 more source

Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis [PDF]

, 2002
Background Disaccharide Intolerance Type I (Mendelian Interance in Man database: *222900) is a rare inborn error of metabolism resulting from mutation in sucrase-isomaltase (Enzyme Catalyzed 3.2.1.48).
Morriss Michael C, Moore Warren H, Baker Susan S, Taylor William, Reid Barbara, Belmont John W, Podrebarac Susan M, Glass Nancy, Schwartz I David   +8 more
core   +1 more source

Narcolepsy and rapid eye movement sleep

Journal of Sleep Research, Volume 34, Issue 2, April 2025.
Summary Since the first description of narcolepsy at the end of the 19th Century, great progress has been made. The disease is nowadays distinguished as narcolepsy type 1 and type 2. In the 1960s, the discovery of rapid eye movement sleep at sleep onset led to improved understanding of core sleep‐related disease symptoms of the disease (excessive ...
Francesco Biscarini, Lucie Barateau, Fabio Pizza, Giuseppe Plazzi, Yves Dauvilliers   +4 more
wiley   +1 more source

The coexistence of hypercalcemia and hypoglycemia in a patient with a renal tumor and B cell lymphoma

Archives of Endocrinology and Metabolism, 2016
SUMMARY Paraneoplastic syndromes are a heterogeneous group of malignant diseases caused by events which involve endocrine, immune and metabolic aspects and whose symptoms vary according to the substance produced and the primary tumor.
Jimena Soutelo, Sofía Moldes, Cielo Frisone, Laura Salvá, Cecilia Agostinis, Gabriel Faraj   +5 more
doaj   +1 more source

Neurological complications of immune checkpoint inhibitors: what happens when you \u27take the brakes off\u27 the immune system. [PDF]

, 2018
Patients with advanced malignancies treated with immune checkpoint inhibitors are at increased risk for developing immune-related neurological complications.
Dalakas, Marinos
core   +1 more source

Prevalence and Prognostic Impact of the Coexistence of Cachexia and Sarcopenia in Patients With Chronic Liver Diseases

Journal of Cachexia, Sarcopenia and Muscle, Volume 17, Issue 3, June 2026.
ABSTRACT Background Cachexia and sarcopenia are prevalent, inflammation‐linked syndromes in chronic liver disease that worsen outcomes. To our knowledge, their coexistence in a single chronic liver disease cohort has not been systematically examined.
Takatsugu Tanaka, Goki Suda, Masatsugu Ohara, Daisuke Yokoyama, Shoichi Kitano, Osamu Maehara, Tomoka Yoda, Qingjie Fu, Zijian Yang, Naohiro Yasuura, Akimitsu Meno, Takashi Sasaki, Risako Kohya, Takashi Kitagataya, Naoki Kawagishi, Masato Nakai, Takuya Sho, Shunsuke Ohnishi, Naoya Sakamoto   +18 more
wiley   +1 more source