Results 51 to 60 of about 6,528 (217)
Multi-organ IgG4-related sialadenitis diagnosed via core needle biopsy: A case report
Advances in Oral and Maxillofacial SurgeryDiagnosing Immunoglobulin G4-related sialadenitis (IgG4-RS) remains challenging due to its rarity and similarity to other forms of sclerosing sialadenitis. Controversies persist regarding biopsy approaches.
Shishuo Ma, Xiaojuan He, Weijia Huang
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Multisystem Mucosal Morbidity in Recessive Dystrophic Epidermolysis Bullosa Inversa
Pediatric Dermatology, EarlyView.ABSTRACT Background/Objectives Recessive dystrophic epidermolysis bullosa inversa (RDEB‐I) is a rare subtype of dystrophic epidermolysis bullosa (EB) characterized by intertriginous cutaneous involvement and frequent mucosal disease. Although mucosal involvement is recognized in RDEB‐I, its cumulative clinical burden remains poorly defined.
Valerie R. Stichert +5 more
wiley +1 more source
Endocrinology, Diabetes &Metabolism, Volume 9, Issue 5, September 2026.Routine radioactive iodine (RAI) after thyroidectomy in low‐risk differentiated thyroid cancer shows no clear benefit in reducing recurrence or improving survival. These findings support a selective, risk‐based approach, avoiding unnecessary treatment and potential adverse effects.
Maheen Asif +5 more
wiley +1 more source
Clinical Medicine Insights: Gastroenterology, 2012 Salivary gland enlargement following the administration of iodine is an extremely rare event, and the pathophysiology of iodine-induced sialadenitis is not yet fully known.
Homam Alkaied +3 more
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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 +8 more
wiley +1 more source
Recurrent neonatal suppurative submandibular sialadenitis: a case report
B-ENT, 2018 Recurrent neonatal suppurative submandibular sialadenitis: a case report. Case report: We describe a case of a premature infant born at 28 1/7 weeks of gestation who, 12 days after birth, developed a submandibular inflammatory mass with exudation of pus ...
N. Albrecht +3 more
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Clinical Case Reports, 2019 Surgical excision of the submandibular salivary gland in patients with chronic sclerosing sialadenitis can be complicated because of hyalinosis of the surrounding soft tissues.
Anna Poghosyan +4 more
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Vegetable twig causing obstructive parotid sialadenitis
CHRISMED Journal of Health and Research, 2016 We report the case of a 4-year-old boy with obstructive parotid sialadenitis in whom the classic clinical presentation clinched the diagnosis which highlights the importance of applied anatomy and clinical examination even in the present age of novel ...
Jonathan Theodore Gondi, Suhasini Gazula
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Ocular facial myositis and sialadenitis presenting with new onset ulcerative colitis
JPGN Reports, Volume 7, Issue 3, Page 436-438, August 2026.Abstract Extra‐intestinal manifestations of inflammatory bowel disease (IBD) can involve most organ systems, although the immunologic underpinnings are not well understood. Most patients who present with an extra‐intestinal manifestation have a single site of extra‐intestinal involvement; however, a small cohort presents with multiple different sites ...
Nicole Du, Nicole Mendez, Anil Darbari
wiley +1 more source
A case of sialadenitis observed as an irAE of atezolizumab: A case report
Respiratory Medicine Case ReportsVarious symptoms emerge as immune-related adverse events of immune checkpoint inhibitor (ICI).A 73-year-old woman, a non-smoker, receiving chemotherapy including atezolizumab for lung adenocarcinoma, presented with fever, bilateral parotid swelling and ...
Kosumi Kumagai +7 more
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