No abstractCEN Case Rep. 2026 Jan 23;15(1):34. doi: 10.1007/s13730-025-01064-4.NO ABSTRACTPMID:41571866 | DOI:10.1007/s13730-025-01064-4
J Formos Med Assoc. 2026 Jan 21:S0929-6646(26)00041-0. doi: 10.1016/j.jfma.2026.01.023. Online ahead of print.ABSTRACTHereditary transthyretin amyloidosis (ATTRv) is a fatal autosomal dominant disorder caused by pathogenic variants in the TTR gene. Various variants cause destabilization of transthyr
Praxis (Bern 1994). 2025 Dec;114(12):434-437. doi: 10.23785/PRAXIS.2025.12.007.ABSTRACTSchnitzler syndrome is a rare autoinflammatory disease that primarily manifests in adulthood. In cases presenting with chronic urticaria and paraproteinemia, Schnitzler syndrome should be considered in the differe
Indian J Pathol Microbiol. 2026 Jan 21. doi: 10.4103/ijpm.ijpm_76_25. Online ahead of print.ABSTRACTAmyloid fibrils aggregate and deposit in many tissues and multiple organs, leading to systemic amyloidosis. One of the main forms of systemic amyloidosis is called amyloid A (AA) amyloidosis, where ch
Curr Probl Diagn Radiol. 2026 Jan 13:S0363-0188(26)00003-4. doi: 10.1067/j.cpradiol.2026.01.003. Online ahead of print.ABSTRACTMammography is traditionally regarded as a domain confined to the detection of breast malignancies; however, it can also serve as a mirror for diverse systemic, haematologic
Curr Probl Cardiol. 2026 Jan 19:103263. doi: 10.1016/j.cpcardiol.2026.103263. Online ahead of print.ABSTRACTBACKGROUND: Transthyretin cardiac amyloidosis (ATTR-CM) is an increasingly recognized cause of heart failure with preserved ejection fraction (HFpEF); however, early diagnosis remains challeng
JACC Case Rep. 2025 Dec 30:106595. doi: 10.1016/j.jaccas.2025.106595. Online ahead of print.ABSTRACTBACKGROUND: Grade 2 or 3 uptake on 99mTc-pyrophosphate scintigraphy is a cornerstone for diagnosing transthyretin amyloidosis. However, light-chain amyloidosis can infrequently mimic this pattern, cau
Ann Med. 2026 Dec;58(1):2617767. doi: 10.1080/07853890.2026.2617767. Epub 2026 Jan 21.ABSTRACTBACKGROUND: The optimal dosing schedule for daratumumab (Dara) in newly diagnosed systemic light-chain (AL) amyloidosis requires refinement. This real-world study compared the efficacy and safety of a frequ
Korean Circ J. 2025 Nov 11. doi: 10.4070/kcj.2025.0421. Online ahead of print.ABSTRACTAtrial cardiomyopathy is a progressive condition that promotes atrial fibrillation (AF) persistence and adverse outcomes. Although fibrosis has long been considered its hallmark, the histopathological basis in non-
Sr Care Pharm. 2026 Jan 1;41(1):3-12. doi: 10.4140/TCP.n.2026.3.ABSTRACTWith the increasing prevalence of polypharmacy, age-related physiological changes, and the need for individualized pharmacotherapy in older patients, understanding new drug approvals is crucial to optimizing medication managemen
J Neurol. 2026 Jan 21;273(2):90. doi: 10.1007/s00415-026-13626-2.ABSTRACTCerebral amyloid angiopathy (CAA) is a common small vessel disease characterized by Aβ deposition in cortical and leptomeningeal arteries, leading to lobar intracerebral hemorrhage and vascular cognitive impairment. Despite adv
No abstractBone Marrow Transplant. 2026 Jan 20. doi: 10.1038/s41409-025-02796-8. Online ahead of print.NO ABSTRACTPMID:41559396 | DOI:10.1038/s41409-025-02796-8
JACC Adv. 2026 Jan 19;5(2):102545. doi: 10.1016/j.jacadv.2025.102545. Online ahead of print.ABSTRACTBACKGROUND: Lumbar spinal stenosis (LSS) and carpal tunnel syndrome (CTS) often predate transthyretin amyloid cardiomyopathy.OBJECTIVE: The aim of this study was to determine if patients with LSS/CTS
Clin Rheumatol. 2026 Jan 20. doi: 10.1007/s10067-025-07798-x. Online ahead of print.ABSTRACTBACKGROUND: Renal involvement in juvenile idiopathic arthritis (JIA) is uncommon (observed in 8.5% of our cohort) and may arise from either the disease itself or its medications. However, differences in renal
No abstractAm J Ophthalmol. 2026 Jan 17:S0002-9394(26)00023-1. doi: 10.1016/j.ajo.2026.01.017. Online ahead of print.NO ABSTRACTPMID:41554420 | DOI:10.1016/j.ajo.2026.01.017
Curr Probl Cardiol. 2026 Jan 17:103265. doi: 10.1016/j.cpcardiol.2026.103265. Online ahead of print.ABSTRACTTransthyretin-mediated (ATTR) and immunoglobulin light-chain (AL) cardiac amyloidosis causes progressive myocardial dysfunction and poor prognosis. Disease-specific therapies in ATTR and anti-
J Neurol. 2026 Jan 19;273(2):86. doi: 10.1007/s00415-026-13618-2.ABSTRACTBACKGROUND: While atrial fibrillation is the leading cause of cardioembolic stroke in elderly patients, the underlying cardiac substrate often remains unidentified. Transthyretin cardiac amyloidosis (ATTR-CA), a treatable cardi
Turk Neurosurg. 2025 Jan 20. doi: 10.5137/1019-5149.JTN.47959-24.2. Online ahead of print.ABSTRACTAmyloidosis is a progressive disorder marked by the deposition of insoluble fibrillar proteins that aggregate in various tissues, leading to tissue damage. Localized amyloidosis, known as amyloidoma, is
J Am Heart Assoc. 2026 Jan 20;15(2):e045558. doi: 10.1161/JAHA.125.045558. Epub 2026 Jan 19.ABSTRACTBACKGROUND: Irregular hematoma border is a prominent yet understudied imaging feature of cerebral amyloid angiopathy (CAA)-related intracerebral hemorrhage (ICH). We investigated whether island sign a
Respir Med Case Rep. 2025 Dec 26;59:102353. doi: 10.1016/j.rmcr.2025.102353. eCollection 2026.ABSTRACTPulmonary amyloidosis presents in nodular, tracheobronchial, and diffuse alveolar-septal forms. Nodular pulmonary amyloidosis (NPA) is usually localized and asymptomatic. It is often linked to indol
Radiol Case Rep. 2026 Jan 5;21(3):1330-1337. doi: 10.1016/j.radcr.2025.12.003. eCollection 2026 Mar.ABSTRACTWild-type transthyretin amyloidosis is a disease characterized by deposition of transthyretin amyloid protein in systemic organs and tissues, especially the heart, lungs, tenosynovium, and lig
Semin Ophthalmol. 2026 Feb;41(2):331-341. doi: 10.1080/08820538.2025.2548021. Epub 2025 Aug 26.ABSTRACTPURPOSE: To describe common ocular surface lesions that clinically mimic ocular surface squamous neoplasia (OSSN) and provide practical guidance for their accurate identification using anterior seg
Alzheimers Dement. 2026 Jan;22(1):e71030. doi: 10.1002/alz.71030.ABSTRACTINTRODUCTION: Cerebral amyloid angiopathy (CAA), marked by amyloid beta (Aβ) accumulation in perivascular spaces (PVSs), contributes to vascular injury and inflammation in Alzheimer's disease. The mechanisms underlying CAA-rela
No abstractInt J Cardiovasc Imaging. 2026 Jan 19. doi: 10.1007/s10554-026-03614-y. Online ahead of print.NO ABSTRACTPMID:41549185 | DOI:10.1007/s10554-026-03614-y
