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1.
Dermatol Ther ; 33(2): e13259, 2020 03.
Article in English | MEDLINE | ID: mdl-32043723

ABSTRACT

We present a series of three kidney transplant patients developing epidermoid cysts after receiving oral tacrolimus for long-term prevention of rejection of the allograft. Cyclosporin A has been known to show this cutaneous adverse drug reaction, but this is the first series of patients with epidermoid cysts following tacrolimus to the best of our knowledge.


Subject(s)
Epidermal Cyst , Kidney Transplantation , Cyclosporine , Epidermal Cyst/chemically induced , Epidermal Cyst/diagnosis , Graft Rejection , Humans , Immunosuppressive Agents/adverse effects , Kidney Transplantation/adverse effects , Tacrolimus/adverse effects
2.
Hautarzt ; 70(5): 363-366, 2019 May.
Article in German | MEDLINE | ID: mdl-30694354

ABSTRACT

Eruptive epidermoid cysts are a rare adverse event of imiquimod treatment for basal cell carcinoma. Up to date, 8 cases have been described in the literature. We present the case of a 75-year-old Caucasian woman with recurrent basal cell carcinoma on the nose. After multiple excisions and treatment with vismodegib, imiquimod 5% cream was administered 5 times per week over 6 weeks. Two months after the end of treatment, the patient presented with eruptive epidermoid cysts.


Subject(s)
Antineoplastic Agents , Carcinoma, Basal Cell , Epidermal Cyst , Imiquimod , Skin Neoplasms , Aged , Aminoquinolines , Antineoplastic Agents/adverse effects , Carcinoma, Basal Cell/drug therapy , Epidermal Cyst/chemically induced , Female , Humans , Imiquimod/adverse effects , Skin Neoplasms/drug therapy , Treatment Outcome
3.
J Eur Acad Dermatol Venereol ; 32(8): 1368-1372, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29575357

ABSTRACT

BACKGROUND: Patients treated with vemurafenib for metastatic melanoma often develop skin lesions similar to those observed after exposure to dioxin-like compounds. We previously called these lesions MADISH (metabolizing acquired dioxin-induced skin hamartoma) when analysing a case of acute dioxin poisoning. OBJECTIVE: We performed a clinical trial aimed at comparing the skin lesions observed under vemurafenib treatment with MADISH in order to bring to light a possible crosstalk between vemurafenib and dioxin pathways. METHODS: In this case series study, we explored the histological aspect of skin lesions in 10 cases treated with vemurafenib for malignant melanoma. We also analysed the ability of vemurafenib and tyrosine kinase inhibitors to induce dioxin-AhR pathway. RESULTS: All patients had skin lesions diagnosed as 'non-inflammatory acneiform eruption' by dermatologists. These were predominantly facial with notable retroauricular involvement and clinically compatible with chloracne/MADISH when assessed by dioxin expert. Histological analysis showed mostly comedone-like lesions and dermal cysts containing epithelial wall with basal or lateral epithelial projections and lamellar keratinization and alterations of remaining sebaceous glands. The expression of CYP1A1, a gene highly induced following dioxin exposure, was not observed in these lesions. Vemurafenib and the tyrosine kinase inhibitors erlotinib and gefitinib did not induce CYP1A1 activity. DISCUSSION: Although the skin lesions under vemurafenib treatment were morphologically similar to MADISH, the absence of CYP1A1 expression in dermal cysts of patients and the absence of CYP1A1 activation by vemurafenib led us consider that these skin lesions were different from true MADISH and not mediated by a crosstalk of AhR signalling, but rather to a hyperactivation of PI3K-Akt pathway as a consequence of vemurafenib treatment. A strong expression of CYP1A1 in the epithelial wall of dermal cysts must be required, parallel to the morphology of the lesions, to make the diagnosis of MADISH, the hallmark of an exposure to dioxin-like/chloracnegen compounds.


Subject(s)
Antineoplastic Agents/adverse effects , Chloracne/pathology , Epidermal Cyst/metabolism , Melanoma/drug therapy , Skin Neoplasms/drug therapy , Vemurafenib/adverse effects , Antineoplastic Agents/pharmacology , Chloracne/etiology , Chloracne/metabolism , Cytochrome P-450 CYP1A1/metabolism , Dioxins/adverse effects , Drug Eruptions/etiology , Drug Eruptions/metabolism , Drug Eruptions/pathology , Enzyme Activation/drug effects , Epidermal Cyst/chemically induced , Erlotinib Hydrochloride/pharmacology , Female , Gefitinib/pharmacology , Hep G2 Cells , Humans , Male , Protein Kinase Inhibitors/pharmacology , Vemurafenib/pharmacology
5.
Anticancer Res ; 36(1): 111-20, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26722034

ABSTRACT

A single intraperitoneal injection of 50 or 75 mg/kg N-methyl-N-nitrosourea in male Sprague-Dawley rats at 4 weeks of age, dose-dependently resulted in cutaneous epithelial cysts and tumors of pilosebaceous origin. Cysts were composed of epidermal cysts or mixed epidermal and inner root sheath hybrid cysts. The majority of induced tumors were keratoacanthomas. A few tumors were trichofolliculomas, trichoblastomas, pilomatricomas, or sebaceous adenomas. All tumors were benign pilosebaceous tumors. Keratoacanthomas were crater-shaped tumors with thick infoldings of epithelium containing keratohyalin granules (epidermal lip) that abruptly changed to epithelium containing trichohyalin granules. The morphological similarity and resemblance of keratin 1, 10, and 14 profiles, and p63 and ß-catenin expression between mixed epidermal and inner root sheath hybrid cysts and keratoacanthomas suggests that hybrid cysts progressed to keratoacanthomas, and the cells from infundibular cells to inner root sheath cells of the pilar segment seem to be the origin of rat keratoacanthomas. Immunohistochemical localization of keratins 1, 10 and 14, p63, and ß-catenin in trichofolliculoma, trichoblastoma, and pilomatricoma, as well as keratoacanthoma, may indicate tumor histogenesis.


Subject(s)
Epidermal Cyst/chemically induced , Keratoacanthoma/chemically induced , Methylnitrosourea , Neoplasms, Glandular and Epithelial/chemically induced , Skin Neoplasms/chemically induced , Skin/drug effects , Animals , Biomarkers, Tumor/metabolism , Disease Models, Animal , Epidermal Cyst/metabolism , Epidermal Cyst/pathology , Humans , Immunohistochemistry , Keratoacanthoma/metabolism , Keratoacanthoma/pathology , Male , Neoplasms, Glandular and Epithelial/metabolism , Neoplasms, Glandular and Epithelial/pathology , Rats, Sprague-Dawley , Skin/metabolism , Skin/pathology , Skin Neoplasms/metabolism , Skin Neoplasms/pathology
8.
J Drugs Dermatol ; 11(10): e35-8, 2012 Oct.
Article in English | MEDLINE | ID: mdl-23134996

ABSTRACT

Enfuvirtide belongs to a newer class of antiretroviral (ARV) agents called fusion inhibitors for the treatment of human immunodeficiency virus type 1 (HIV-1) infection. Enfuvirtide blocks attachment, binding, and entry of the viral capsid into the host CD4+ cell. Administration is only available subcutaneously in a twice-daily regimen particularly for those patients who have previously failed more than one ARV regimen. Common side effects of enfuvirtide administration include fatigue, insomnia, nausea, and diarrhea; however, injection-site reactions are the most common side effect and present in nearly all individuals undergoing treatment. The spectrum of cutaneous manifestations ranges from little to no reaction to cysts, nodules, induration, or sclerodermalike lesions. These reactions are mostly variants of iatrogenically induced hypersensitivity and are self-limited.


Subject(s)
Drug Eruptions/pathology , Epidermal Cyst/chemically induced , HIV Envelope Protein gp41/adverse effects , HIV Fusion Inhibitors/adverse effects , HIV Infections/drug therapy , HIV-1 , Peptide Fragments/adverse effects , Cysts/chemically induced , Drug Eruptions/etiology , Enfuvirtide , Erythema/chemically induced , HIV Envelope Protein gp41/pharmacokinetics , HIV Envelope Protein gp41/therapeutic use , HIV Fusion Inhibitors/pharmacokinetics , HIV Fusion Inhibitors/therapeutic use , Humans , Injections, Subcutaneous , Patient Selection , Peptide Fragments/pharmacokinetics , Peptide Fragments/therapeutic use , Pruritus/chemically induced
9.
Dermatology ; 215(4): 352-3, 2007.
Article in English | MEDLINE | ID: mdl-17911995

ABSTRACT

A 61-year-old woman developed multiple and clustered eruptive epidermoid cysts at the site of treatment of a basal cell carcinoma located on her nose with imiquimod 5% cream (5 times/week for 6 weeks). Clearing was achieved after topical treatment with tretinoin 0.025% cream (1 application/day for 1 month).


Subject(s)
Aminoquinolines/adverse effects , Antineoplastic Agents/adverse effects , Epidermal Cyst/chemically induced , Nose , Aminoquinolines/therapeutic use , Antineoplastic Agents/therapeutic use , Biopsy , Carcinoma, Basal Cell/drug therapy , Carcinoma, Basal Cell/pathology , Diagnosis, Differential , Epidermal Cyst/pathology , Facial Neoplasms/drug therapy , Facial Neoplasms/pathology , Female , Follow-Up Studies , Humans , Imiquimod , Middle Aged
12.
Toxicol Pathol ; 24(5): 564-72, 1996.
Article in English | MEDLINE | ID: mdl-8923677

ABSTRACT

An international workshop of toxicologic pathologists reviewed cystic keratinizing squamous lesions of the rat lung. These lesions develop in response to the chronic inhalation of diverse particulate materials. Controversy exists over the biological significance of these changes and their relevance to humans. For the first time, in one place, a group of pathologists analyzed slides from all available studies. The workshop reached a consensus as to classification of these unique pulmonary tissue responses and offers diagnostic criteria for application. Although additional research is needed, this working classification scheme should serve as a practical interim approach for pathologists and regulatory agencies.


Subject(s)
Epidermal Cyst/classification , Epidermal Cyst/pathology , Keratins/analysis , Lung Diseases/classification , Lung Diseases/pathology , Animals , Carcinoma, Squamous Cell/pathology , Epidermal Cyst/chemically induced , Epithelium/drug effects , Epithelium/pathology , Lung Diseases/chemically induced , Lung Neoplasms/pathology , Rats , Rats, Inbred F344 , Rats, Sprague-Dawley , Rats, Wistar , Xenobiotics/toxicity
13.
Cancer Res ; 55(19): 4479-85, 1995 Oct 01.
Article in English | MEDLINE | ID: mdl-7671263

ABSTRACT

The timing of intestinal tumor initiation in B6-Min/+ mice has been examined by treating mice at 5-35 days of age with a single i.p. injection of the direct-acting alkylating agent N-ethyl-N-nitrosourea (ENU). Treatment of Min/+ mice at 5-14 days of age resulted in a 3.8-fold increase in intestinal tumor multiplicity over untreated mice. Mice treated at 20-35 days of age showed only a 1.6-fold increase in tumor number. These results, in conjunction with examination of tumor multiplicities of untreated Min/+ mice as a function of age, suggest that the majority of intestinal tumors in Min/+ mice are initiated relatively early in life. Min/+ mice treated with ENU also showed an increase in the number of cystic intestinal crypts. However, the relationship between age at ENU treatment and cystic crypt multiplicity was distinct from that seen for intestinal adenomas. Mice treated at 5-9 days of age showed only a 1.9-fold increase in cystic crypts over untreated animals. By contrast, the increase in average cystic crypt multiplicity for mice treated at 10-35 days of age was 4.5-fold. In addition, 60% of Min/+ mice treated with ENU before 25 days of age developed epidermoid cysts, an extracolonic manifestation commonly associated with familial adenomatous polyposis in humans.


Subject(s)
Adenoma/chemically induced , Carcinogens/toxicity , Cysts/chemically induced , Epidermal Cyst/chemically induced , Ethylnitrosourea/toxicity , Intestinal Diseases/chemically induced , Intestinal Neoplasms/chemically induced , Skin Neoplasms/chemically induced , Age Factors , Animals , Female , Male , Mice
14.
Cell Struct Funct ; 19(5): 335-40, 1994 Oct.
Article in English | MEDLINE | ID: mdl-7850895

ABSTRACT

The localization of estrogen receptors (EsR) in the tumor tissues of submandibular glands was examined in female rats, using the indirect immunoperoxidase method in combination with the in situ hybridization technique. Tumors were experimentally produced by 9,10-dimethyl-1,2-benzanthracene (DMBA), and the tumor tissues were fixed with formalin or paraformaldehyde and then embedded in paraffin. In the DMBA-induced submandibular gland tumors, immunoreactivity to EsR-peroxidase conjugate was found in nuclei of the tumor cells which occupied the peripheral rim of the tumor cell nests. In contrast, the reactivity in the normal submandibular glands without tumor was mostly confined to nuclei of the duct cells. When EsR mRNA expression was analyzed in the tumor tissue by in situ hybridization with a cDNA probe, its distribution was identical with that of immunoreactivity to EsR. These data suggest that the ductal cells of the submandibular gland are responsive to ovarial steroids, and that estrogens may play an important role in the maintenance of growth of the submandibular gland tumors.


Subject(s)
Carcinoma, Squamous Cell/chemistry , Epidermal Cyst/metabolism , Receptors, Estrogen/analysis , Submandibular Gland Diseases/metabolism , Submandibular Gland Neoplasms/chemistry , 9,10-Dimethyl-1,2-benzanthracene , Animals , Carcinoma, Squamous Cell/chemically induced , Carcinoma, Squamous Cell/pathology , Cell Nucleus/chemistry , Cell Nucleus/ultrastructure , DNA Probes/analysis , DNA Probes/genetics , DNA, Complementary/analysis , DNA, Complementary/genetics , Epidermal Cyst/chemically induced , Epidermal Cyst/pathology , Female , Immunohistochemistry , In Situ Hybridization , RNA, Messenger/analysis , RNA, Messenger/genetics , Rats , Rats, Inbred F344 , Receptors, Estrogen/genetics , Receptors, Estrogen/physiology , Submandibular Gland Diseases/chemically induced , Submandibular Gland Diseases/pathology , Submandibular Gland Neoplasms/chemically induced , Submandibular Gland Neoplasms/pathology
15.
Hautarzt ; 44(8): 521-3, 1993 Aug.
Article in German | MEDLINE | ID: mdl-8376106

ABSTRACT

A 66-year-old man was treated with cyclosporin A (Sandimmun) after a kidney transplant and developed numerous epidermal cysts, comedones and folliculitis in the 2nd year of the immunosuppressive therapy. The eruptions were more marked on the back and in the temporal and retroauricular regions of the face. Histological examination of a cystic tumour revealed a follicular cyst of the acro-infundibular type. While hypertrichosis and gingival hyperplasia are now well known as side effects of cyclosporin A, cystic and acneiform skin lesions must also be attributed to this drug.


Subject(s)
Cyclosporine/adverse effects , Epidermal Cyst/chemically induced , Folliculitis/chemically induced , Kidney Transplantation , Postoperative Complications/chemically induced , Acne Vulgaris/chemically induced , Acne Vulgaris/pathology , Aged , Biopsy , Cyclosporine/administration & dosage , Epidermal Cyst/pathology , Folliculitis/pathology , Humans , Male , Postoperative Complications/pathology , Skin/pathology
16.
Cutis ; 50(1): 36-8, 1992 Jul.
Article in English | MEDLINE | ID: mdl-1516377

ABSTRACT

A forty-two-year-old male recipient of a cadaver renal transplant showed multiple nodulocystic lesions on his back and lateral aspects of his neck four months after beginning immunosuppressive therapy with cyclosporine A and prednisone. Results of histopathologic studies revealed that they were epidermoid infundibular cysts. We note the relationship between this clinical appearance and cyclosporine A, as well as this agent's cutaneous side effects.


Subject(s)
Cyclosporine/adverse effects , Epidermal Cyst/chemically induced , Kidney Transplantation , Skin Diseases/chemically induced , Adult , Cyclosporine/pharmacology , Epidermal Cyst/pathology , Humans , Male , Skin Diseases/pathology
17.
J Am Acad Dermatol ; 25(5 Pt 2): 940-3, 1991 Nov.
Article in English | MEDLINE | ID: mdl-1761775

ABSTRACT

Both topical nitrogen mustard and psoralen photochemotherapy may induce benign and malignant alterations in the skin. We describe the explosive appearance of multiple epidermal cysts and squamous cell carcinomas in a patient whose cutaneous T-cell lymphoma was treated sequentially with these two types of therapy. This is the first report of both processes in the same patient with cutaneous T-cell lymphoma. It strongly supports the concept of lesion induction, while raising the question of an additive or even synergistic effect of these types of therapy.


Subject(s)
Carcinoma, Squamous Cell/chemically induced , Epidermal Cyst/chemically induced , Lymphoma, T-Cell, Cutaneous/drug therapy , Mechlorethamine/adverse effects , Skin Diseases/chemically induced , Skin Neoplasms/drug therapy , Administration, Cutaneous , Carcinoma, Squamous Cell/pathology , Epidermal Cyst/pathology , Humans , Male , Middle Aged , PUVA Therapy/adverse effects , Skin Diseases/pathology , Skin Neoplasms/chemically induced
18.
J Am Acad Dermatol ; 21(2 Pt 1): 215-7, 1989 Aug.
Article in English | MEDLINE | ID: mdl-2768571

ABSTRACT

Milia developed in two patients with different chronic dermatoses after 2 weeks of treatment with clobetasol propionate ointment. Routine histologic and immunohistochemical analysis showed the cysts to be of eccrine gland origin.


Subject(s)
Betamethasone/analogs & derivatives , Clobetasol/adverse effects , Epidermal Cyst/chemically induced , Skin Diseases/drug therapy , Administration, Topical , Aged , Epidermal Cyst/pathology , Female , Humans , Male , Middle Aged
19.
Br J Dermatol ; 119(6): 743-50, 1988 Dec.
Article in English | MEDLINE | ID: mdl-3144317

ABSTRACT

We carried out a clinicopathological study of epithelial cutaneous lesions induced in Dunkin-Hartley albino guinea-pigs by means of the topical application of 7,12-dimethyl-benzanracene. By the end of the study we had observed 4451 lesions. Most frequently observed were epithelial hyperplasia and dysplasia (2544 lesions). Neoplasias consisted of 244 carcinomas in situ, and 88 squamous carcinomas. Basal-cell epitheliomas were few. Epidermal cysts were a frequent finding.


Subject(s)
9,10-Dimethyl-1,2-benzanthracene , Disease Models, Animal , Guinea Pigs , Skin Neoplasms/chemically induced , Animals , Carcinoma in Situ/chemically induced , Carcinoma, Basal Cell/chemically induced , Carcinoma, Squamous Cell/chemically induced , Epidermal Cyst/chemically induced , Epithelium/pathology , Hyperplasia/chemically induced , Male , Skin/pathology , Skin Diseases/chemically induced , Skin Neoplasms/pathology
20.
Am J Otolaryngol ; 7(5): 360-5, 1986.
Article in English | MEDLINE | ID: mdl-3490800

ABSTRACT

The temporal bones of a newborn infant with hydantoin syndrome showed multiple middle ear and inner ear anomalies. There was a constellation of bony and membranous defects involving the oval and round windows, cochlear ducts, cochlear aqueducts, endolymphatic ducts and sacs, and vestibular labyrinths. To the authors' knowledge, supernumerary vestibular sensory epithelial structures and an inner ear epidermoid cyst have not been previously reported. Wide communications between the subarachnoid space and inner ear were of surgical relevance.


Subject(s)
Abnormalities, Drug-Induced/etiology , Ear, Inner/abnormalities , Ear, Middle/abnormalities , Hydantoins/adverse effects , Adult , Cochlear Aqueduct/abnormalities , Cochlear Duct/abnormalities , Ear Neoplasms/chemically induced , Ear Neoplasms/congenital , Endolymphatic Duct/abnormalities , Endolymphatic Sac/abnormalities , Epidermal Cyst/chemically induced , Epidermal Cyst/congenital , Epilepsy/drug therapy , Female , Humans , Infant, Newborn , Male , Oval Window, Ear/abnormalities , Pregnancy , Pregnancy Complications/drug therapy , Round Window, Ear/abnormalities , Syndrome , Vestibule, Labyrinth/abnormalities
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