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5.
J Cutan Med Surg ; 19(3): 317-9, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25775647

RESUMO

BACKGROUND: Tophaceous gout is the nonarticular deposition of monosodium urate resulting from a disorder in purine metabolism that causes an elevation of serum uric acid. Cutaneous variants of tophaceous gout include papular, nodular, ulcerative, and pustular forms. OBJECTIVE: We present a case of a 67-year-old man who presented with multiple cutaneous creamy white papules and nodules. A biopsy was taken, and a diagnosis of cutaneous tophaceous gout was made. The treatment and pathophysiology are discussed. CONCLUSION: Miliarial gout is a rare form of cutaneous tophaceous gout that is treated using xanthine oxidase inhibitors such as allopurinol and febuxostat or uricosurics such as probenecid.


Assuntos
Gota/diagnóstico , Miliária/diagnóstico , Idoso , Gota/patologia , Humanos , Masculino , Miliária/patologia , Coxa da Perna/patologia
6.
J Eur Acad Dermatol Venereol ; 29(1): 7-13, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25124255

RESUMO

BACKGROUND: Benign lesions of the breast in total are much more frequent than malignant ones. However, there are no epidemiologic data on the prevalence of benign or malignant tumours of the nipple, and the bibliography on benign nipple tumours in general is limited. AIMS: To present some rare cases of benign nipple tumours and review the literature. MATERIALS AND METHODS: Four cases of rare benign nipple tumours: neurofibromas, wart, leiomyoma and milium are presented. The literature search on benign nipple tumours was performed using MEDLINE, Pubmed, and Cochrane databases with limits: English language, human species and available abstract. The keyword used was 'benign nipple tumours'. RESULTS: The initial search retrieved 337 articles. The papers were reviewed and the articles that referred to benign lesions that appeared at the nipple specifically were identified. Different entities that were described included: neurofibroma, leiomyoma, milium, florid papillomatosis, syringomatous adenoma, nevoid hyperkeratosis, fibroma, pseudolymphoma and haemangioma. DISCUSSION: Differential diagnosis of benign tumours of the nipple can be demanding for the physicians. Many of the symptoms and signs like pruritus, serosanguinous discharge, lichenification, erosion and nodular enlargement are produced by either malignant or benign nipple lesions. Radiology can be unclear in the diagnosis of nipple abnormalities. CONCLUSION: Histological examination of the lesion can be the only definite answer in these cases.


Assuntos
Neoplasias da Mama/patologia , Leiomioma/patologia , Neurofibromatose 1/patologia , Mamilos , Neoplasias Cutâneas/patologia , Verrugas/patologia , Adulto , Feminino , Humanos , Lactente , Leiomioma/química , Pessoa de Meia-Idade , Miliária/diagnóstico , Papiloma/diagnóstico , Pseudolinfoma/diagnóstico , Doenças Raras , Siringoma/diagnóstico , Verrugas/cirurgia
8.
Skinmed ; 12(4): 250-1, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25335356

RESUMO

A 64-year-old man presented with asymptomatic eruption on his right forearm and the dorsum of the hand present for 2 weeks. There was no history of trauma, prolonged sun exposure, or application of or contact with any substance prior to the development of lesions. He was a known hypertensive and diabetic and was taking treatment for these conditions. The rest of his history was noncontributory. On examination, multiple grouped tiny white papules were found on both normal skin and on the erythematous plaque. These papules were of almost uniform size (2-4 mm) and were notable for absence of umbilication. The erythematous plaque was roughly 15 cm in length and was extending along the ulnar border of forearm and dorsum of hand in a linear pattern (Figure 1). The surface temperature of the plaque appeared similar to the surrounding area, and the surface was studded with multiple tiny white papules. There were no lesions suggestive of chronic actinic damage in the surrounding area. The papules revealed solid whitish material on expression with a needle. The rest of the mucocutaneous examination was noncontributory. Based on clinical presentation, a diagnosis of linear milia en plaque was made.


Assuntos
Miliária/patologia , Dermatopatias/patologia , Antebraço , Mãos/patologia , Humanos , Ceratose , Masculino , Pessoa de Meia-Idade , Miliária/diagnóstico , Dermatopatias/diagnóstico
10.
Pediatrics ; 133(5): e1373-6, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24709934

RESUMO

Milia are benign, superficial keratinaceous cysts that present as fine, small white papules. Milia en plaque is a rare, challenging-to-treat variant most often seen in the posterior auricular region. A total of 9 cases of milia en plaque have been reported in the pediatric literature to date. We report a case of milia en plaque of the nose in a 7-year-old boy, a novel site of involvement in the pediatric population, and successful treatment with the use of topical tretinoin. Topical retinoids offer an effective treatment option for the management of milia en plaque in the pediatric population.


Assuntos
Miliária/tratamento farmacológico , Doenças Nasais/tratamento farmacológico , Tretinoína/administração & dosagem , Administração Tópica , Criança , Dermoscopia , Esquema de Medicação , Humanos , Ceratose , Masculino , Miliária/diagnóstico , Doenças Nasais/diagnóstico , Resultado do Tratamento
12.
Cutis ; 91(4): 191-2, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23763079

RESUMO

Multiple eruptive milia (MEM) is a rare skin condition characterized by sudden onset of multiple milia occurring mainly on the head, neck, and trunk. Milia are small, benign, 1- to 4-mm, white keratinous cysts. The lesions generally are asymptomatic and may arise spontaneously or secondary to a number of processes. Multiple eruptive milia are cosmetically troublesome and difficult to treat. We report the case of a 40-year-old man with an abrupt onset of MEM on the face.


Assuntos
Dermatoses Faciais/patologia , Miliária/patologia , Retinoides/uso terapêutico , Administração Cutânea , Adulto , Fármacos Dermatológicos/administração & dosagem , Fármacos Dermatológicos/uso terapêutico , Dermatoses Faciais/diagnóstico , Dermatoses Faciais/tratamento farmacológico , Seguimentos , Humanos , Ceratose , Masculino , Miliária/diagnóstico , Miliária/tratamento farmacológico , Retinoides/administração & dosagem
13.
JAMA Dermatol ; 149(4): 436-8, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23715198

RESUMO

IMPORTANCE: In 1947, Sulzberger and colleagues published a micrograph of a blocked acrosyringium in a patient with atopic dermatitis (AD), believing that it had a large role in the disease process. Lacking appropriate probes, they could not confirm the finding. OBJECTIVE: To confirm the observations by Sulzberger et al on the blockage of sweat ducts in AD in pathologic specimens. DESIGN AND SETTING: Biopsy specimens diagnostic of various inflammatory diseases and with a secondary differential diagnosis of eczema were evaluated at an academic medical center. EXPOSURES: Evidence of ductal obstruction in each specimen was examined following staining with hematoxylin-eosin, periodic acid-Schiff, and Gram stain. MAIN OUTCOMES AND MEASURES: Comparison of biopsy specimens with control specimens and additional controls consisting of noninflamed skin. RESULTS: Using 36 biopsy specimens, this study confirmed the observations by Sulzberger et al on the blockage of sweat ducts in AD. Blocked acrosyringia were noted in each specimen on routine staining with hematoxylin-eosin. The study also confirmed the findings by earlier investigators about the blockage of sweat ducts in miliaria, showing eosinophilic material in the ducts that was positive for periodic acid-Schiff. Previous researchers also observed bacteria in the blockages, and this study demonstrated the same findings in AD, rather than miliaria. CONCLUSION AND RELEVANCE: Subclinical miliaria may be the earliest change in AD and likely initiates the process that causes intense pruritus.


Assuntos
Dermatite Atópica/etiologia , Miliária/complicações , Glândulas Sudoríparas/patologia , Biópsia , Dermatite Atópica/diagnóstico , Diagnóstico Diferencial , Progressão da Doença , Humanos , Miliária/diagnóstico , Reprodutibilidade dos Testes
15.
Pediatr Dermatol ; 30(4): e48-51, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-22276567

RESUMO

Two infants presented with multiple asymptomatic papules and geographic and annular plaques over the extensor aspect of the upper and lower extremities and trunk. Skin biopsy of both lesions showed plugged and hyperplastic dilated acrosryingia and deep dermal ducts, along with granulomatous inflammatory reaction. These lesions showed self-healing with complete resolution. A previous report described similar clinical and histopathologic features and labeled it giant centrifugal miliaria profunda. Because of the large granulomatous plaques and deep infiltrate, we propose that it was a granulomatous variant of giant centrifugal miliaria profunda. We report these cases for their rarity and self-healing nature.


Assuntos
Miliária/classificação , Miliária/diagnóstico , Índice de Gravidade de Doença , Pele/patologia , Cicatrização , Biópsia , Feminino , Humanos , Lactente , Masculino , Remissão Espontânea
16.
Pediatr Dermatol ; 30(2): 263-4, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-22276686

RESUMO

Milia-like idiopathic calcinosis cutis (MICC) is a rare dermopathy, usually occurring in children with Down syndrome. We report a case of an 8-year-old girl with Down syndrome who presented with histologically verified MICC, briefly review the literature on MICC, discuss the differential diagnosis, and describe the use of dermoscopy in the evaluation of lesions, which we believe has never been published previously with this entity.


Assuntos
Calcinose/diagnóstico , Síndrome de Down/complicações , Miliária/diagnóstico , Dermatopatias/diagnóstico , Pele/patologia , Calcinose/patologia , Criança , Dermoscopia , Diagnóstico Diferencial , Síndrome de Down/diagnóstico , Feminino , Humanos , Dermatopatias/patologia
17.
Curr Opin Pediatr ; 24(4): 472-9, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22790100

RESUMO

PURPOSE OF REVIEW: Diaper dermatitis is the most common cutaneous diagnosis in infants. In this review, common causes of diaper dermatitis and similarly presenting conditions will be covered, as well as updates on treatments of common diaper dermatitides. RECENT FINDINGS: There have been recent advancements in the treatment of diaper dermatitis. In addition, there are many newly recognized causes of diaper dermatitis that clinicians should be aware of. SUMMARY: Irritant dermatitis is the most common cause of diaper dermatitis. However, there are multiple other common causes of diaper dermatitis and it is thus imperative that the clinician be aware of cutaneous mimickers of irritant diaper dermatitis as well as their treatments.


Assuntos
Acrodermatite/patologia , Dermatite das Fraldas/patologia , Doença de Mão, Pé e Boca/patologia , Histiocitose de Células de Langerhans/patologia , Miliária/patologia , Líquen Escleroso Vulvar/patologia , Acrodermatite/complicações , Acrodermatite/diagnóstico , Candidíase Cutânea/patologia , Dermatite Seborreica/patologia , Diagnóstico Diferencial , Dermatite das Fraldas/diagnóstico , Dermatite das Fraldas/etiologia , Feminino , Doença de Mão, Pé e Boca/complicações , Doença de Mão, Pé e Boca/diagnóstico , Humanos , Lactente , Recém-Nascido , Masculino , Miliária/complicações , Miliária/diagnóstico , Psoríase/patologia , Infecções Estafilocócicas/patologia , Infecções Estreptocócicas/patologia , Líquen Escleroso Vulvar/complicações , Líquen Escleroso Vulvar/diagnóstico , Zinco/deficiência
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