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Anal squamous cell carcinoma (SqCC) can be broadly divided into HPV-positive and HPV-negative groups, each with distinct clinicopathologic features and outcome. CYLD-mutant anal SqCC was recently characterized as having a strong association with cylindroma-like histologic features, HPV positivity, infrequent PIK3CA mutation, and low tumor mutational burden. The prognostic impact of CYLD mutation in this context has not been established. We performed CYLD mutational analysis on a cohort of 109 clinicopathologically well-characterized cases of anal SqCC including 98 HPV-positive and 11 HPV-negative carcinomas. CYLD mutation was present in 3 cases (2.8 % of total, 3.1 % of HPV-positive cases), all of which were HPV16-positive. CYLD mutation was significantly associated with more frequent cylindroma-like basement membrane inclusions (p = 0.0002) and basaloid cytomorphology (p = 0.017). Just 4 % of CYLD-wildtype carcinomas demonstrated cylindroma-like features, which were limited in extent relative to CYLD-mutant cases. Among the HPV-positive group, CYLD mutation and cylindroma-like morphology were associated with a higher rate of metastatic disease progression (p = 0.022 and p = 0.01, respectively), with 2 of 3 CYLD-mutant patients developing liver metastasis at 6 and 7 months after initial diagnosis. None of the CYLD-mutant cases had other mutations including PIK3CA and TP53 mutations. Our findings further establish CYLD-mutant anal SqCC as an infrequent but distinct clinicopathologic entity with characteristic pathogenetic features and a possible association with adverse clinical outcomes. Among HPV-positive anal SqCC, CYLD mutation represents a potentially useful novel marker for this distinct entity and cylindroma-like morphology serves as a useful feature to identify such cases.
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http://dx.doi.org/10.1016/j.humpath.2025.105765 | DOI Listing |
Virchows Arch
September 2025
DERMPATH Muenchen, Munich, Germany.
Benign lymphoepithelial tumors of salivary glands had been restricted to sebaceous and non-sebaceous (NSLA) lymphadenomas. However, salivary neoplasms recapitulating carcinoma showing thymus-like elements (CASTLE) have been the subject of recent case reports. We reviewed clinicopathological, immunohistochemical, and molecular findings in 20 salivary gland tumors with thymus-like phenotype (18 histologically benign and two with malignant component).
View Article and Find Full Text PDFAm J Dermatopathol
July 2025
PathWest Dermatopathology, PathWest Laboratory Medicine, J Block, QEII Medical Centre, Perth, WA, Australia.
Cylindrocarcinoma is a very rare malignant adnexal neoplasm. The diagnosis of cylindrocarcinoma typically requires identifying a precursor benign component; indeed the current World Health Organization classification classifies these lesions within the group of malignant neoplasms arising from cylindroma. We present a unique case of architecturally low-grade pure cylindrocarcinoma, supported by striking morphologic and immunohistochemical features and showing an inactivating CYLD1 mutation.
View Article and Find Full Text PDFFish Shellfish Immunol
October 2025
Research Institute of Life Sciences, Gyeongsang National University, Jinju, 52828, South Korea; Division of Applied Life Science (BK21 Four), Gyeongsang National University, Jinju, 52828, South Korea; Division of Life Science, Gyeongsang National University, Jinju, 52828, South Korea. Electronic add
The deubiquitinase cylindromatosis (CYLD) negatively regulates the MAPK and NF-κB signaling pathways by removing ubiquitin from upstream regulatory elements in the TLR pathway. Although the regulatory mechanisms of mammalian CYLD are well-characterized, its function in TLR signaling pathways in fish is still largely unexplored. Herein, we investigated the function of CYLD in modulating the TLR response in rainbow trout (Oncorhynchus mykiss).
View Article and Find Full Text PDFItal J Pediatr
May 2025
Department of Medical Genetics and Prenatal Diagnosis, Sichuan Provincial Women's and Children's Hospital, Chengdu, Sichuan, 610045, China.
Background: Balanced chromosomal rearrangements (BCRs) are common structural variations (SVs), but only a small number of individuals with BCRs exhibit abnormalities. To better understand the different phenotypes in children diagnosed with BCRs during the prenatal period, we plan to thoroughly investigate the SVs and evaluate their pathogenicity in five children with BCRs.
Methods: Five children with BCRs detected through karyotyping and chromosome microarray analysis (CMA) during prenatal diagnoses were analyzed using SVseq technology.
J Invest Dermatol
May 2025
INSERM U981, Gustave Roussy Cancer Campus, Université Paris Saclay, Villejuif, France. Electronic address:
CYLD cutaneous syndrome (CCS) is a rare genetic disorder caused by germline CYLD mutations, leading to multiple benign skin tumors, including cylindromas, spiradenomas, and trichoepitheliomas. Although these tumors are well-characterized histologically, their molecular landscape remains unclear, and no targeted treatments exist. To comprehensively analyze the molecular features of CCS tumors, we integrated newly generated and publicly available data using multiomic approaches.
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