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1.
Head Neck Pathol ; 7(1): 64-8, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23054955

RESUMEN

Differentiation of salivary gland acinic cell carcinoma from mucoepidermoid carcinoma can be diagnostically challenging as both may have prominent mucin production. P63 is a p53 homologue required for limb and epidermal morphogenesis. It is expressed in basal and myoepithelial cells of normal salivary gland tissues. In this immunohistochemical study, we examined the expression of p63 in salivary gland acinic cell and mucoepidermoid carcinomas (MEC) and its use in differentiating these two entities. A search was performed and appropriate cases were selected from Lifespan Hospital System archives as well as the consult archives of one author (DRG). 31 salivary gland acinic cell carcinomas (ACC) and 24 MEC were examined for p63 expression by immunohistochemistry. The nuclear immunoreactivity was examined by both authors and was graded semi-quantitatively with negative being less than 10 % of cells staining. Positive staining was graded as follows: 10-25 % of tumor cells staining was weakly positive, 26-75 % of tumor cells staining was moderately positive, and 76-100 % of tumor cells staining was strongly positive. Negative nuclear staining of the tumor cells was seen in 30/31 (96 %) of salivary gland ACC while 1/31 (3 %) showed diffuse nuclear staining of the tumor cells. This latter case was later reclassified as mammary analogue secretory carcinoma following confirmatory molecular testing for the ETV6-NTRK3 fusion gene. Strong positive nuclear staining of the tumor cells was seen in 24 (100 %) of salivary gland MEC cases. P63 is an immunohistochemical stain that can potentially aid in differentiating unusual ACC with prominent mucin production from MEC of the salivary gland. According to this study, acinic cell carcinoma is always negative for p63 immunoreactivity while mucoepidermoid carcinoma is always positive.


Asunto(s)
Carcinoma de Células Acinares/diagnóstico , Carcinoma Mucoepidermoide/diagnóstico , Proteínas de la Membrana/biosíntesis , Neoplasias de las Glándulas Salivales/diagnóstico , Biomarcadores de Tumor/análisis , Carcinoma de Células Acinares/metabolismo , Carcinoma Mucoepidermoide/metabolismo , Diagnóstico Diferencial , Humanos , Neoplasias de las Glándulas Salivales/metabolismo
3.
Semin Arthritis Rheum ; 41(3): 434-44, 2011 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21868067

RESUMEN

OBJECTIVE: We describe 4 patients who presented with palpable purpura, arthralgia or arthritis, leukopenia, and antineutrophil cytoplasmic antigen (ANCA) positivity most likely as a result of a hypersensitivity reaction to cocaine-levamisole induced vasculopathy. METHODS: Cases were seen and reviewed in both the inpatient consult service and the outpatient clinics at Rhode Island Hospital from August 2009 to August 2010. Clinical characteristics as well as pertinent laboratory parameters were also reviewed and corroborated with a review of the present literature. RESULTS: We describe 3 cases of cocaine-levamisole-related cutaneous vasculitis with or without associated neutropenia, and 1 case of severe neutropenia with oral mucosal ulceration. Further serologic studies revealed maximum titers of ANCA mostly in a perinuclear pattern. Antimyeloperoxidase tested negative or mildly elevated in our cohort. Three patients with neutropenia had positive antigranulocyte IgM antibody. Nonsteroidal anti-inflammatory drugs were effective as first-line treatment for joint pain. The use of colchicine and systemic corticosteroid was employed to manage severe and persistent skin lesions. CONCLUSIONS: Cocaine-levamisole-related cutaneous vasculitis with leukopenia is a diagnosis of exclusion, but this diagnosis should be strongly considered in patients with a history of cocaine abuse who present with a tetrad of cutaneous manifestations consisting of palpable purpura or bullae with ear involvement, arthralgias, leukopenia, and positive ANCA in high titers and negative Antimyeloperoxidase, when other infectious or idiopathic vasculitic entities have been excluded.


Asunto(s)
Antirreumáticos/efectos adversos , Cocaína/efectos adversos , Inhibidores de Captación de Dopamina/efectos adversos , Leucopenia/inducido químicamente , Levamisol/efectos adversos , Vasculitis Leucocitoclástica Cutánea/inducido químicamente , Femenino , Humanos , Leucopenia/inmunología , Leucopenia/patología , Masculino , Persona de Mediana Edad , Púrpura/inducido químicamente , Púrpura/inmunología , Púrpura/patología , Vasculitis Leucocitoclástica Cutánea/inmunología , Vasculitis Leucocitoclástica Cutánea/patología
6.
Pediatr Infect Dis J ; 27(8): 762-4, 2008 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-18664989

RESUMEN

The current standard of care for a fungal central venous catheter infection in a pediatric patient usually requires removal without any other feasible options. Although removal may reduce the rate of Candida-associated complications, literature reviews question whether the outcomes of removal substantiate this being the standard of care. We report 6 cases of central venous catheter fungal infections treated with liposomal amphotericin-B lock therapy. These cases consisted of 4 patients, 2 of whom received recurrent therapy. In 4 of these cases, there was successful eradication of the infectious fungal agent, allowing continued use of the catheter. A controlled study of antifungal lock therapy should be considered as a potential alternative to removal.


Asunto(s)
Anfotericina B/uso terapéutico , Antifúngicos/uso terapéutico , Candidiasis/tratamiento farmacológico , Cateterismo Venoso Central/efectos adversos , Fungemia/tratamiento farmacológico , Liposomas/uso terapéutico , Anfotericina B/administración & dosificación , Antifúngicos/administración & dosificación , Sangre/microbiología , Candida albicans/efectos de los fármacos , Candida albicans/aislamiento & purificación , Candida glabrata/efectos de los fármacos , Candida glabrata/aislamiento & purificación , Candidiasis/microbiología , Niño , Medios de Cultivo , Femenino , Fungemia/microbiología , Humanos , Lactante , Liposomas/administración & dosificación , Masculino , Resultado del Tratamiento
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