Superficial suppurative necrolytic dermatitis in a miniature schnauzer associated with the application of an imidacloprid and flumethrin collar.

Superficial suppurative necrolytic dermatitis (SSND) of miniature schnauzers is a rare cutaneous and visceral reaction pattern associated with shampoo. This report describes SSND in a miniature schnauzer associated with application of an imidacloprid and flumethrin collar. Histopathology was consistent with SSND. Lesions resolved after treatment with methylprednisolone and marbofloxacin.

La dermatite nécrolytique suppurative superficielle (SSND) des schnauzers miniatures est un patron réactionnel viscéral et cutané rare associé au shampooing. Cet article décrit SSND chez un schnauzer miniature associé à l'application d'un collier d'imidaclopride et de fluméthrine. L'histopathologie était compatible avec SSND. Les lésions se sont résolues après traitement avec méthylprednisolone et marbofloxacine.

La dermatitis necrolítica supurativa superficial (SSND) de los Schnauzer miniatura es un patrón de reacción cutánea y visceral poco común descrito en asociación con algunos champúes. Este informe describe SSND en un Schnauzer miniatura asociado con la aplicación de un collar de imidacloprid y flumetrina. La histopatología fue compatible con SSND. Las lesiones se resolvieron tras el tratamiento con metilprednisolona y marbofloxacina.

A dermatite necrolítica supurativa superficial (DNSS) de schnauzers miniatura é um raro padrão reacional cutâneo e visceral associado ao uso de shampoos. Este relato descreve um caso de DNSS em um schnauzer miniatura associado à aplicação de uma coleira de imidaclorprida e flumetrina. A histopatologia foi consistente com DNSS. As lesões foram resolvidas após o tratamento com metilprednisolona e marbofloxacino.

Alternative therapies in veterinary dermatology.

This article presents an overview of alternative therapies for skin disorders including traditional Chinese medicine (acupuncture and Chinese herbs), homeopathy, and Western herbs and plant extracts. The medical and veterinary literature on the aforementioned modalities will be reviewed with a focus on reduction of inflammation and pruritus of the skin and ear canal in the canine species. Clinical application and potential adverse effects will also be included when available.

Bexarotene blunts malignant T-cell chemotaxis in Sezary syndrome: reduction of chemokine receptor 4-positive lymphocytes and decreased chemotaxis to thymus and activation-regulated chemokine.

The malignant cells in Sezary syndrome express the skin trafficking molecules' cutaneous lymphocyte associated antigen (CLA) and chemokine receptor 4 (CCR4). High levels of the CCR4 ligand, thymus, and activation-regulated chemokine (TARC), have been reported in the blood and skin of patients. The rexinoid X-receptor specific retinoid, bexarotene, has contributed to the resolution of cutaneous disease among patients. To evaluate the effects of bexarotene on skin trafficking molecule expression and chemotaxis, peripheral blood mononuclear cells from Sezary syndrome patients and healthy controls were treated with bexarotene in vitro. CCR4 and CLA expression levels and chemotaxis in response to TARC (6.25 ng/ml) were evaluated among lymphocytes before and after treatment with bexarotene (10 microM). Flow cytometric analysis was performed to evaluate CD4, CD26, CLA, and CCR4 cell surface expression. Transwell migration assays were performed to evaluate chemotaxis to TARC. Prior to treatment, malignant cells exhibited higher CCR4 expression (45-90%) and greater than four times more chemotaxis to TARC compared with healthy controls. After treatment with bexarotene for 36-96 hr, a 28% reduction in CCR4 expression was noted (P < 0.05) among the malignant population with an associated 9% decrease in chemotaxis to TARC (P < 0.05). Our results show that bexarotene may inhibit malignant cell trafficking to the skin through an ability to suppress CCR4 expression among Sezary syndrome lymphocytes.

Biological effects of bexarotene in cutaneous T-cell lymphoma.

OBJECTIVE: To determine the effects of bexarotene on malignant T cells isolated from the peripheral blood of patients with the leukemic variant of cutaneous T-cell lymphoma (Sézary syndrome). DESIGN, SETTING, AND PARTICIPANTS: Peripheral blood mononuclear cells from 9 patients with Sézary syndrome and a high burden of circulating malignant T cells (>50% of peripheral blood mononuclear cells) and 6 healthy volunteers underwent evaluation at a university medical center, to test the effects of bexarotene on T cells. MAIN OUTCOME MEASURES: The capacity of bexarotene to induce apoptosis and its effects on T-cell cytokine production from peripheral blood lymphocytes isolated from patients with Sézary syndrome. RESULTS: Bexarotene produced dose-dependent apoptosis of peripheral blood T cells from patients with Sézary syndrome. The T cells from approximately two thirds of patients were consistently sensitive to bexarotene, whereas those from the remaining one third of patients were consistently resistant to the apoptotic effects of bexarotene. Bexarotene inhibited mitogen-induced interleukin 4 production by the peripheral blood cells of patients with Sézary syndrome, and this effect correlated with sensitivity of patients' cells to apoptosis. In contrast to the retinoic acid receptor-specific retinoid, all-trans retinoic acid, bexarotene does not induce the augmentation of interferon gamma production. CONCLUSIONS: Bexarotene induces apoptosis of malignant T cells from patients with Sézary syndrome, but the cells from a proportion of patients are resistant to the apoptotic effects. Interleukin 4 production, which can play a role in the systemic immunosuppression that characterizes advancing Sézary syndrome, may be inhibited by bexarotene.

The use of cytokines, fusion proteins and antibodies to treat cutaneous T-cell lymphoma.

It has long been known that certain immune augmenting therapeutics, particularly interferon alpha, can exert profound salutary effects on the clinical progress of patients with cutaneous T-cell lymphoma. Emerging evidence that the host immune response may play an important role in the control of this disorder has led to the clinical application of other cytokines including interleukin-12 and interferon gamma. In this review, the authors will summarize current knowledge regarding the use of cytokines, fusion proteins and antibodies for the treatment of cutaneous T-cell lymphoma.

Acute necrotizing dermatitis and septicemia after application of a d-limonene-based insecticidal shampoo in a cat.

A 2-year-old female spayed domestic shorthair cat was examined because of lethargy, inappetance, vocalization, and abnormal aggressive behavior of 1 day's duration. The cat had been groomed the previous day with a d-limonene-based insecticidal shampoo. Skin lesions consisted of coalescing erythematous patches. Despite supportive care, the cat's condition deteriorated. Dermatohistopathologic changes included multifocal areas of acute coagulative epidermal necrosis. The dermis was infiltrated by a dense population of bacilli. d-Limonene toxicosis has been rarely described in dogs and cats. Toxic effects such as hypersalivation, ataxia, shivering, hypothermia, scrotal irritation, hypotension, and erythema multiforme major have been reported. Treatment for septicemia and disseminated intravascular coagulation, along with intensive supportive care, may be necessary.

Cytokines and other biologic agents as immunotherapeutics for cutaneous T-cell lymphoma.

Cutaneous T-cell lymphomas (CTCLs) are a group of skin-invasive malignancies of clonally derived T lymphocytes. Mycosis fungoides and Sézary syndrome, characterized by the proliferation of CD4+ T cells, are the most common forms of CTCL. Among these latter disorders, the host antitumor response appears to play an important role in disease control. Thus, systemic therapeutic agents are used in an effort to augment the host antitumor response while selectively targeting the malignant cells. Both new and old biologic response-modifying treatment options currently used to treat CTCL are reviewed.