PMID- 34958303 OWN - NLM STAT- MEDLINE DCOM- 20220401 LR - 20220401 IS - 0722-5091 (Print) IS - 0722-5091 (Linking) VI - 41 IP - 2 DP - 2022 Mar-Apr TI - Cerebral amyloidomas: Perspective on unusual morphological features. PG - 46-52 LID - 10.5414/NP301440 [doi] AB - AIMS: Cerebral amyloidomas (CAs) are mass-producing congophilic lesions most commonly due to lambda light chain deposits, contrasting them with light chain deposition disease (LCDD) which has non-polarizable, often kappa light chain deposition. MATERIALS AND METHODS: Although usual histological features are well known, we detail 3 recent CAs with unusual morphological findings and review the literature specifically for these features. RESULTS: Two women, aged 56 and 58 years, had right cerebral white matter CAs. The biopsy of case 1 disclosed congophilic polarizable deposits with prominent dystrophic mineralization as well as scant plasma cells. Case 2 had a CA with significant multinucleated giant cell reaction to the amyloid and additionally contained an area suspicious for marginal zone B-cell lymphoma. Case 3 was a clinically unsuspected CA identified at autopsy in a 75-year-old woman that manifested as several contiguous left frontal lobe white matter erythematous, hyperemic lesions; microscopy showed nodular and concentric amyloid deposits and thick perivascular cuffs of plasma cells. Mass spectrometry proved lambda light and alpha heavy chain amyloid deposits in all 3 cases. CONCLUSION: These 3 CA cases illustrate several unusual gross and microscopic features that are discussed in context with the literature. FAU - Kleinschmidt-DeMasters, Bette K AU - Kleinschmidt-DeMasters BK LA - eng PT - Case Reports PT - Journal Article PL - Germany TA - Clin Neuropathol JT - Clinical neuropathology JID - 8214420 RN - 0 (Amyloid) SB - IM MH - Aged MH - Amyloid/analysis MH - *Amyloidosis/diagnosis/pathology MH - Female MH - Humans MH - *Lymphoma, B-Cell/pathology MH - Middle Aged MH - Plasma Cells/pathology MH - *Soft Tissue Neoplasms/pathology EDAT- 2021/12/28 06:00 MHDA- 2022/04/02 06:00 CRDT- 2021/12/27 12:13 PHST- 2022/02/10 00:00 [accepted] PHST- 2021/12/28 06:00 [pubmed] PHST- 2022/04/02 06:00 [medline] PHST- 2021/12/27 12:13 [entrez] AID - 189088 [pii] AID - 10.5414/NP301440 [doi] PST - ppublish SO - Clin Neuropathol. 2022 Mar-Apr;41(2):46-52. doi: 10.5414/NP301440.