• A Case of Muir-Torre Syndrome
• A case of multiple self-healing squamous epitheliomas of Ferguson-Smith in a patient on systemic immunosuppression for rheumatoid arthritis
• A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings
• A new mutation in Muir-Torre syndrome associated with familiar transmission of different gastrointestinal adenocarcinomas
• A puzzling case: SCC or not?
• A rare case of axillary keratoacanthoma arising in hidradenitis suppurativa
• Aberrant expression of S100A6 and matrix metalloproteinase 9, but not S100A2, S100A4, and S100A7, is associated with epidermal carcinogenesis
• Amphiregulin overexpression results in rapidly growing keratinocytic tumors: an in vivo xenograft model of keratoacanthoma
• Biallelic MYH germline mutations as cause of Muir-Torre syndrome
• Breast Cancer Pathological Image Classification Based on the Multiscale CNN Squeeze Model
• Cancer-associated genodermatoses
• Case no. 8. Bullous dermatosis
• Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review
• Colorectal cancer and the Muir-Torre syndrome in a Gypsy family: a review
• Common benign skin tumors
• Comparative analysis of the expression of ERBIN and Erb-B2 in normal human skin and cutaneous carcinomas
• Cutaneous adverse effects of targeted therapies: Part II: Inhibitors of intracellular molecular signaling pathways
• Cutaneous metastases masquerading as solitary or multiple keratoacanthomas
• Cutaneous sebaceous neoplasms as markers of Muir-Torre syndrome: a diagnostic algorithm
• Cystatin M / E expression in inflammatory and neoplastic skin disorders
• Dermoscopic Features of Giant Molluscum Contagiosum in a Patient with Acquired Immunodeficiency Syndrome
• Diagnosing Common Benign Skin Tumors
• Different phenotypes in Muir-Torre syndrome: clinical and biomolecular characterization in two Italian families
• Differential expression of cell survival and cell cycle regulatory proteins in cutaneous squamoproliferative lesions
• Digenic/multilocus aetiology of multiple self-healing squamous epithelioma (Ferguson-Smith disease): TGFBR1 and a second linked locus
• Distinct variants affecting differential splicing of TGFBR1 exon 5 cause either Loeys-Dietz syndrome or multiple self-healing squamous epithelioma
• Dowling-Degos Disease with Hidradenitis Suppurativa and Inflammatory Arthritis in Two Generations
• Elevated cutaneous Smad activation associates with enhanced skin tumor susceptibility in organ transplant recipients
• Evaluation of universal immunohistochemical screening of sebaceous neoplasms in a service setting
• Expression of stromelysin 3 in keratoarcanthoma and squamous cell carcinoma
• Expression of the Ly6/uPAR-domain proteins C4.4A and Haldisin in non-invasive and invasive skin lesions
• Expression pattern of the bcl-2 homologous protein bad in normal skin, psoriasis vulgaris and keratinocytic tumors
• Family with MSH2 mutation presenting with keratoacanthoma and precancerous skin lesions
• Features of multiple self-healing squamous epithelioma and Loeys-Dietz syndrome in a patient with a novel TGFBR1 variant
• Generalized eruptive keratoacanthoma of Grzybowski
• Generalized eruptive keratoacanthoma: a diagnostic and therapeutic challenge
• Generalized eruptive keratoacanthomas of Grzybowski: A case report followed over 11 years
• Giant keratinized chalazion masquerading as a keratoacanthoma in a child
• Grzybowski's generalized eruptive keratocanthomas: a case report
• Hereditary non-polyposis colorectal cancer associated with disseminated superficial porokeratosis. Microsatellite instability in skin tumours
• Human Orf: An Under-recognized Entity
• Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: role of clinical features, microsatellite instability, and immunohistochemistry
• Imiquimod 5 percent cream and the treatment of cutaneous malignancy
• Immunoexpression of Bcl-x in squamous cell carcinoma and keratoacanthoma: differences in pattern and correlation with pathobiology
• Immunohistochemistry screening of sebaceous lesions for Muir-Torre syndrome in a 26-year period in a Mexican population
• Incidence of xeroderma pigmentosum in Larkana, Pakistan: a 7-year study
• Incontinentia pigmenti with painful subungual tumors: a two-generation study
• Keratinisation disorders: new data
• Keratoacanthoma (KA): An update and review
• Keratoacanthoma or cutaneous squamous cell carcinoma revealing a DNA mismatch repair default (Muir-Torre Syndrome)
• Keratoacanthoma: a clinico-pathologic enigma
• Lynch syndrome with exclusive skin involvement: time to consider a molecular definition?
• Lynch syndrome, Muir Torre variant: 2 cases
• Lynch Syndrome: Current management In 2019
• Metachronous cutaneous squamous cell carcinoma in a young patient as the only presenting symptom to uncover Lynch syndrome with MLH1 Germline mutation
• Microsatellite instability and immunostaining for MSH-2 and MLH-1 in cutaneous and internal tumors from patients with the Muir-Torre syndrome
• Mismatch repair proteins expression and microsatellite instability in skin lesions with sebaceous differentiation: a study in different clinical subgroups with and without extracutaneous cancer
• Molecular pathologic analysis enhances the diagnosis and management of Muir-Torre syndrome and gives insight into its underlying molecular pathogenesis
• Muir-Torre syndrome
• Muir-Torre syndrome
• Muir-Torre syndrome - treatment with isotretinoin and interferon alpha-2a can prevent tumour development
• Muir-Torre syndrome (MTS): An update and approach to diagnosis and management
• Muir-Torre syndrome and familial colorectal cancer: 2 families with molecular genetic analysis
• Muir-Torre Syndrome and founder mismatch repair gene mutations: A long gone historical genetic challenge
• Muir-Torre syndrome associated with endometrial carcinoma
• Muir-Torre syndrome: case report of a patient with concurrent jejunal and ureteral cancer and a review of the literature
• Muir-Torre Syndrome: The Importance of a Detailed Family History
• Multiple and aggressive keratoacanthomas associated with Ferguson-Smith syndrome, successfully treated by cetuximab and cisplatin
• Multiple familial keratoacanthoma of Witten and Zak - A report of three siblings
• Multiple keratoacanthomas in a patient with myelodysplastic syndrome
• Multiple keratoacanthomas in a young woman: report of a case emphasizing medical management and a review of the spectrum of multiple keratoacanthomas
• Multiple keratoacanthomas of Ferguson-Smith type
• Multiple self-healing palmoplantar carcinoma: a familial predisposition to skin cancer with primary palmoplantar and conjunctival lesions
• Multiple self-healing scarring lesions on the face
• Multiple self-healing squamous epithelioma (MSSE): rare variants in an adjacent region of chromosome 9q22.3 to known TGFBR1 mutations suggest a digenic or multilocus etiology
• Multiple self-healing squamous epithelioma in different ethnic groups: more than a founder mutation disorder?
• Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1
• Multiple self-healing squamous epithelioma of Ferguson-Smith: observations in a Danish family covering four generations
• Multiple self-healing squamous epithelioma, or Ferguson-Smith disease: demonstration of mutations in the TGFβ-receptor
• Mutation in the MSH2 gene in Muir-Torre syndrome
• Myxofibrosarcoma harboring an MLH1 pathogenic germline variant associated with Muir-Torre syndrome: a case report
• New facial papules in a 66-year-old woman with bladder cancer
• Nodular Melanoma Mimicking Keratoacanthoma: Lessons to learn
• Non-familial multiple keratoacanthomas in a 70 year-old long-term non-progressor HIV-seropositive man
• Recognising and treating. Premalignant skin conditions
• Sebaceous skin lesions as clues to hereditary non-polyposis colorectal cancer
• Severe exacerbation of multiple self-healing squamous epithelioma (Ferguson-Smith disease) with radiotherapy, which was successfully treated with acitretin
• Simultaneous Muir-Torre and Turcot's syndrome: A case report and review of the literature
• Solitary subungual keratoacanthoma arising in an MSH2 germline mutation carrier: confirmation of a relationship by immunohistochemical analysis
• SPONTANEOUSLY HEALING FERGUSON-SMITH EPITHELIOMAS AND MULTIPLE FAMILIAL KERATOACANTHOMAS
• Sporotrichoid Keratoacanthomas: Case Report and Review of Neoplasms Presenting in a Sporotrichoid Pattern
• Successful Treatment of Generalized Eruptive Keratoacanthoma of Grzybowski with Acitretin
• Successful treatment of multiple keratoacanthoma with topical imiquimod and low-dose acitretin
• The liver: another organ involved in Muir Torre syndrome?
• TPM4 promotes cell migration by modulating F-actin formation in lung cancer
• Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is expressed in normal skin and cutaneous inflammatory diseases, but not in chronically UV-exposed skin and non-melanoma skin cancer
• Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas
• Vemurafenib cooperates with HPV to promote initiation of cutaneous tumors
• Web Application for the Automated Extraction of Diagnosis and Site From Pathology Reports for Keratinocyte Cancers
• Xeroderma pigmentosum