Results 31 to 40 of about 4,709 (183)

The clinical challenge of SIADH--three cases [PDF]

Clinical Kidney Journal, 2009
The syndrome of inappropriate antidiuretic hormone secretion (SIADH) remains a challenging disorder to diagnose and treat. Three cases are presented to illustrate these challenges. The first two cases had drug-induced SIADH secondary to a selective serotonin reuptake inhibitor (for depression) or carbamazepine (for trigeminal neuralgia). The third case
Van Der Lubbe, Nils, Thompson, Christopher J., Zietse, Robert, Hoorn, Ewout J.   +3 more
openaire   +3 more sources

Hand Lesions as a Diagnostic Clue in Unexplained SIADH

Clinical Case Reports, Volume 14, Issue 8, August 2026.
Chilblain‐like hand lesions in a patient with otherwise unexplained SIADH prompted evaluation for autoimmune connective tissue disease. (A) Hand lesions before treatment. (B) Marked improvement after topical difluprednate therapy. (C) Skin biopsy showing basal liquefaction/interface change with superficial perivascular lymphocytic infiltration.
Nobuko Watanabe, Takuya Omura, Takahiro Kamihara, Taiki Sugimoto, Jun Matsumoto, Tomomi Omura, Masaki Hasegawa, Mariko Shimono, Zenzo Isogai   +8 more
wiley   +1 more source

SIADH Associated with Prostate Cancer [PDF]

Electrolyte & Blood Pressure, 2007
Syndrome of inappropriate antidiuretic hormone secretion (SIADH) is the most common disease leading to hyponatremia, and it is characterized by an inappropriately elevated serum ADH level relative to serum osmolality. This syndrome may occur in a variety of clinical settings including malignancies.
Lee, Kyun Sang, Kang, Taek Won, Ma, Seong Kwon, Kim, Soo Wan, Kim, Nam Ho, Choi, Ki Chul   +5 more
openaire   +2 more sources

Secondary Adrenal Insufficiency Presenting With Severe Hyponatremia in an Elderly Patient With Primary Aldosteronism Suggesting Underlying Autonomous Cortisol Secretion

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Possible unrecognized cortisol autonomy in primary aldosteronism may suppress the hypothalamic–pituitary–adrenal axis. Under physiological stress, this may contribute to secondary adrenal insufficiency and severe hyponatremia. Clinicians should consider adrenal insufficiency in patients with primary aldosteronism presenting with unexplained ...
Minami Toda, Shunsuke Takahashi, Hitomi Saito, Honami Mori, Yutaka Kuroda, Akito Maeshima   +5 more
wiley   +1 more source

Survival Outcomes and Complications Among Canadian Children With Retinoblastoma: A Population‐Based Report From CYP‐C

Pediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Purpose Retinoblastoma (RB) is the most common pediatric ocular cancer, yet population‐based data on survival and risk factors remain limited. This study aimed to describe survival in a large national RB cohort and identify predictors of death and complications.
Samuel Sassine, Ofélie Trudeau‐Ferrin, Caroline Laverdière, Patrick Hamel, Rosanne Superstein, Bénédicte Koukoui, Carole Provost, Paul C. Nathan, Vijay Ramaswamy, Furqan Shaikh, Brenda Gallie, Ashwin Mallipatna, Stephanie Kletke, Helen Dimaras, Hallie Coltin   +14 more
wiley   +1 more source

Case Report: Long-Term Tolvaptan Treatment in a Child With SIADH and Suprasellar Arachnoid Cyst

Frontiers in Pediatrics, 2021
Suprasellar arachnoid cysts represent a rare occurrence in the pediatric population and usually cause symptoms related to mass effect and can occasionally cause endocrine dysfunctions.
Andrea Puma, Milena Brugnara, Paolo Cavarzere, Marco Zaffanello, Giorgio Piacentini, Rossella Gaudino   +5 more
doaj   +1 more source

Porphyria‐Safe Emergency Management in COVID‐Associated GBS‐Like Neuropathy: Why Early Medication Review Should Accompany PBG/ALA Testing

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT In COVID‐associated acute neuropathy with abdominal pain, seizures, hyponatremia, hypertension, or hepatic involvement, suspected acute intermittent porphyria should prompt both early PBG/ALA testing and immediate porphyria‐safe medication review to avoid worsening neurovisceral attacks before diagnostic confirmation.
Muhammad Abdullah Awan
wiley   +1 more source

Non‐Small Cell Lung Carcinoma Presenting as Isolated Malignant Ascites in the Absence of a Detectable Primary Tumor: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT An 89‐year‐old woman presented with abdominal distension and altered mental status. Non‐portal‐hypertensive ascites suggested spontaneous bacterial peritonitis, but ascitic‐fluid cytology with immunoprofiling and circulating tumor‐DNA confirmed non‐small cell lung carcinoma despite no detectable primary tumor, underscoring early consideration ...
Angad Tiwari, Ashish Sharma, Monica Lewkowicz, Hareesha Rishab Bharadwaj, Khabab Abbasher Hussien Mohamed Ahmed, Edgar Naut   +5 more
wiley   +1 more source

Use of Tolvaptan in pediatric SIADH associated hyponatremia: A case report

Journal of Pediatric Critical Care
Hyponatremia is a common electrolyte abnormality in pediatric patients, often associated with infections and central nervous system pathology. Syndrome of inappropriate antidiuretic hormone secretion (SIADH) is a frequent cause. We describe the case of a
Sonam Agrawal, Rakesh Kumar, Ashish Simalti, Suprita Kalra   +3 more
doaj   +1 more source

From Metabolic Crisis to Molecular Classification: Multidisciplinary Management of Synchronous Endometrioid Ovarian and Endometrial Carcinomas With Massive Tumor Burden

Cancer Nexus, Volume 2, Issue 3, July 2026.
Managing massive tumor burden in synchronous endometrioid carcinomas. The graphical abstract summarizes the clinical pathway from presentation with massive ascites, pleural effusion, and critical metabolic abnormalities to multidisciplinary stabilization, surgical management, integrated morphologic–molecular classification, and shared decision‐making ...
Anna Homeniuk, Leena Abdalla, Sharon Fitzgerald   +2 more
wiley   +1 more source