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1.
Cutis ; 82(1): 51-4, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18712024

ABSTRACT

We present a 40-year-old man with occupation-induced pemphigus vulgaris (PV). He developed PV within days of a one-time heavy exposure to fumes of burning glyphosate, a broad-spectrum nonselective pesticide. This exposure suggests acute cutaneous contact as a stimulus in the development of his pemphigus. While the patient initially required mycophenolate mofetil and prednisone therapy, he has since eliminated contact with pesticides and has been successfully tapered off systemic medication. We discuss the case and review concepts of inducible PV by pesticides and physical cutaneous injury.


Subject(s)
Glycine/analogs & derivatives , Herbicides/adverse effects , Pemphigus/chemically induced , Adult , Glycine/adverse effects , Humans , Male , Pemphigus/diagnosis , Pemphigus/therapy , Glyphosate
2.
Drugs ; 66(13): 1657-64, 2006.
Article in English | MEDLINE | ID: mdl-16978032

ABSTRACT

Topical immune response modifiers include imiquimod and resiquimod. The mechanism of action of immune response modifiers is complex and not completely understood. It involves the stimulation of innate and cell-mediated immune responses through Toll-like receptor-mediated induction of cytokines. Imiquimod is approved for the treatment of actinic keratoses, superficial basal cell carcinomas and warts; it has also been documented to successfully treat other forms of skin cancer such as squamous cell carcinoma in situ, melanoma and extramammary Paget's disease.


Subject(s)
Adjuvants, Immunologic/therapeutic use , Skin Neoplasms/drug therapy , Adjuvants, Immunologic/administration & dosage , Aminoquinolines/administration & dosage , Aminoquinolines/therapeutic use , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/therapeutic use , Cytokines/metabolism , Humans , Imidazoles/administration & dosage , Imidazoles/therapeutic use , Imiquimod , Models, Biological , Skin Neoplasms/immunology , Skin Neoplasms/pathology , Toll-Like Receptors/physiology
3.
Mod Pathol ; 17(1): 28-32, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14631375

ABSTRACT

Cutaneous eccrine and apocrine glands have many histologic and immunologic similarities to ducts and acini of the breast. Thus, differentiating a primary cutaneous process from a metastatic breast carcinoma can be nearly impossible. In all, 10-34% of breast carcinomas overexpress HER-2 protein, a membrane-associated protein that functions in cell differentiation, adhesion and motility. As expression of this gene in cutaneous neoplasms has not been well characterized, we sought to determine HER-2 expression in a sample of benign and malignant cutaneous eccrine and apocrine neoplasms and to determine if there is value in using this protein expression in differentiating primary cutaneous from metastatic breast lesions. Totally, 85 primary cutaneous neoplasms and 11 cutaneous metastases from HER-2-positive breast carcinomas were retrieved from archived material at our institute. All cases were evaluated for HER-2 protein expression using the Dako Hercept Test kit. Membranous HER-2 staining was noted in three of the 85 cutaneous adnexal neoplasms: one hidrocystoma and two nodular hidradenomas. Seven of the 11 cutaneous metastases from HER-2-positive breast carcinomas maintained moderate-to-strong HER-2 expression. In conclusion, while 10-34% of breast carcinomas overexpress the HER-2 protein, only 3.5% of cutaneous apocrine and eccrine neoplasms in this study stained with the HER-2 antibody. These HER-2-positive cutaneous neoplasms typically do not pose a diagnostic dilemma in the setting of differentiation from breast metastasis. Additionally, although histologically these breast and cutaneous lesions may have morphologic similarities, the relative lack of HER-2 overexpression suggests that they are different nosologically. Finally, this study suggests that HER-2 protein expression can be a useful tool in differentiating a primary cutaneous appendageal neoplasm from HER-2 expressing metastatic breast carcinoma.


Subject(s)
Apocrine Glands/chemistry , Breast Neoplasms/diagnosis , Eccrine Glands/chemistry , Neoplasms, Adnexal and Skin Appendage/pathology , Receptor, ErbB-2/analysis , Sweat Gland Neoplasms/pathology , Adenoma, Sweat Gland/chemistry , Adenoma, Sweat Gland/pathology , Apocrine Glands/pathology , Breast Neoplasms/chemistry , Breast Neoplasms/pathology , Diagnosis, Differential , Eccrine Glands/pathology , Female , Hidrocystoma/chemistry , Hidrocystoma/pathology , Humans , Neoplasms, Adnexal and Skin Appendage/chemistry , Neoplasms, Adnexal and Skin Appendage/secondary , Predictive Value of Tests , Reproducibility of Results , Sweat Gland Neoplasms/chemistry , Sweat Gland Neoplasms/secondary
4.
J Cutan Pathol ; 30(6): 379-81, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12834487

ABSTRACT

BACKGROUND: Epidermolytic hyperkeratosis (EH) is most commonly associated with the diffuse involvement of congenital ichthyosiform erythroderma, but can also be found in a localized pattern. Localized EH is rare, but mucocutaneous lesions have been been identified, most commonly in the mouth. METHODS: We observed a 58-year-old African-American female who noted spots on her genitalia for approximately 2 years. The lesions were increasing in size, darkening, and had become pruritic and sore over the past 6 months. RESULTS: Physical examination revealed seven scattered, tan to brown, verrucoid papules on the labia and mons pubis, resembling condylomata acuminata or Bowenoid papulosis. Biopsy of a single labial papule revealed epidermal acanthosis, compact hyperkeratotic papillomatosis, perinuclear clear zones, granular keratohyalin clumping, hypergranulosis, and dyskeratosis resulting in intracellular eosinophilic globules, all characteristic of EH. CONCLUSIONS: Because of the rarity of localized genital EH and similar appearance to common diagnoses, clinical confusion may occur without biopsy.


Subject(s)
Genitalia, Female/pathology , Hyperkeratosis, Epidermolytic/pathology , Biopsy , Female , Humans , Middle Aged
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