Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 27
Filter
6.
Actas Dermosifiliogr (Engl Ed) ; 111(9): 769-770, 2020 Nov.
Article in English, Spanish | MEDLINE | ID: mdl-32858010
9.
J Cutan Pathol ; 36(6): 660-7, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19515045

ABSTRACT

BACKGROUND: Neonatal lupus erythematosus (NLE) is a disease associated with the transplacental transfer of maternal anti-Ro/SSA. The histopathologic characteristics of neonatal lupus have been described as compatible with cutaneous lupus based on isolated cases. METHODS: We retrospectively review the available literature and compare them with findings obtained in seven biopsies of five cases. RESULTS: Erythematous-desquamative lesions and urticaria-like lesions were observed in our series. Two cases showed both type of lesions. Vacuolar alterations at the dermoepidermal interface and adnexal structures were the histopathologic findings on erythematous-desquamative lesions, and a superficial and deep perivascular and periadnexal lymphocytic infiltrate was the major pattern in urticaria-like lesions. One case showed prevalence of eosinophils in the inflammatory infiltrate. Sixty cases have been reported previously. Sixty-five percent presented erythematous-desquamative and 29% urticaria-like lesions. Pathologic findings of erythematous-desquamative lesions were similar to those found in our series, but epidermal vacuolar changes were the predominant histopathologic finding in urticaria-like lesions of cases reported in the literature. CONCLUSIONS: The majority of cases of NLE show vacuolar alteration at the dermoepidermal interface and adnexal structures. Some cases exhibit a superficial and deep perivascular and periadnexal lymphocytic infiltrate without epidermal alteration, and rare cases may have eosinophils in the infiltrate.


Subject(s)
Lupus Erythematosus, Cutaneous/pathology , Female , Humans , Immunohistochemistry , Infant , Infant, Newborn , Infant, Newborn, Diseases/pathology , Lupus Erythematosus, Cutaneous/metabolism , Male , Retrospective Studies
12.
Protoplasma ; 231(3-4): 145-9, 2007.
Article in English | MEDLINE | ID: mdl-17762907

ABSTRACT

Calcium oxalate crystals are by far the most prevalent and widely distributed mineral deposits in higher plants. In Tradescantia pallida, an evergreen perennial plant widely used as an ornamental plant, calcium oxalate crystals occur in the parenchymal tissues of stem, leaf, and root, as well as in flower organs, in the form of either raphides or tetragonal prismatic crystals or both. Energy-dispersive X-ray analysis revealed that C, O, and Ca were the main elements; and K, Cl, and Si, the minor elements. Infrared and X-ray analyses of crystals collected from these tissues detected the coexistence of two calcium oxalate chemical forms, i.e., whewellite and weddellite, as well as calcite, opal, and sylvite. Here, we show for the first time the occurrence of epitaxy in mineral crystals of plants. Epitaxy, which involves the oriented overgrowth of one crystal onto a second crystalline substrate, might explain how potassium chloride (sylvite)--one of the most water-soluble salts--stays insoluble in crystal form when coated with a calcium oxalate epilayer. The results indicate the potential role of crystals in regulating the ionic equilibrium of both calcium and potassium ions.


Subject(s)
Potassium Chloride/chemistry , Tradescantia/chemistry , Calcium/metabolism , Calcium Oxalate/chemistry , Crystallization , Infrared Rays , Microscopy, Electron, Scanning , Potassium/metabolism , Tradescantia/metabolism , Tradescantia/ultrastructure , X-Ray Diffraction
13.
Actas Dermosifiliogr ; 98(3): 188-93, 2007 Apr.
Article in Spanish | MEDLINE | ID: mdl-17504704

ABSTRACT

We report a case of primary cutaneous infection by Mycobacterium haemophilum after the bite of an aquarium fish in a severely immunodepressed AIDS patient. Clinical features consisted in nodular and ulcerative lesions that followed a sporotrichoid pattern. Histological study of nodular lesions showed a granulomatous dermatitis with numerous acid-fast bacilli. The mycobacterium was identified 3 months later by genetic hybridization from a cultive in solid medium. Combined therapy with isoniazid, rifampin, clarithromycin, ethambutol, amikacin and ciprofloxacin resulted in complete resolution of the lesions. Infection by Mycobacterium haemophilum is a rare mycobacteriosis that usually affects immunodepressed patients. The most common clinical manifestations are cutaneous lesions but the development of sporotrichoid nodular lymphangitis is exceptional.


Subject(s)
AIDS-Related Opportunistic Infections/diagnosis , Finger Injuries/complications , Hand Dermatoses/diagnosis , Mycobacterium Infections/diagnosis , Mycobacterium haemophilum/isolation & purification , Wound Infection/diagnosis , AIDS-Related Opportunistic Infections/drug therapy , AIDS-Related Opportunistic Infections/etiology , AIDS-Related Opportunistic Infections/microbiology , AIDS-Related Opportunistic Infections/pathology , Adult , Animals , Anti-Bacterial Agents/therapeutic use , Antitubercular Agents/therapeutic use , Arm , Arthritis, Infectious/etiology , Bites and Stings/complications , Cichlids , Drug Resistance, Bacterial , Drug Therapy, Combination , Granuloma/diagnosis , Granuloma/etiology , Granuloma/microbiology , Granuloma/pathology , Hand Dermatoses/drug therapy , Hand Dermatoses/etiology , Hand Dermatoses/microbiology , Hand Dermatoses/pathology , Humans , Immunocompromised Host , Leg , Male , Mycobacterium Infections/drug therapy , Mycobacterium Infections/etiology , Mycobacterium Infections/microbiology , Mycobacterium Infections/pathology , Mycobacterium haemophilum/drug effects , Skin Ulcer/etiology , Wound Infection/drug therapy , Wound Infection/etiology , Wound Infection/microbiology
14.
Actas dermo-sifiliogr. (Ed. impr.) ; 98(3): 188-193, abr. 2007. ilus
Article in Es | IBECS | ID: ibc-053208

ABSTRACT

Presentamos un caso de infección primaria cutánea por Mycobacterium haemophilum tras la mordedura de un pez de acuario en un paciente con sida, gravemente inmunodeprimido. Las manifestaciones cutáneas consistieron en lesiones nodulares y ulcerativas que seguían un trayecto esporotricoide. El estudio histológico de las lesiones nodulares mostró una dermatitis granulomatosa con numerosos bacilos ácido-alcohol resistentes. La micobacteria se identificó tres meses después mediante hibridación genética a partir de un cultivo en medio sólido. Se instauró terapia combinada con isoniazida, rifampicina, claritromicina, etambutol, amikacina y ciprofloxacino con curación de las lesiones. La infección por Mycobacterium haemophilum es una micobacteriosis poco frecuente que aparece habitualmente en el paciente inmunodeprimido. Las lesiones cutáneas son las manifestaciones clínicas más frecuentes, pero la presentación en forma de linfangitis nodular esporotricoide es excepcional


We report a case of primary cutaneous infection by Mycobacterium haemophilum after the bite of an aquarium fish in a severely immunodepressed AIDS patient. Clinical features consisted in nodular and ulcerative lesions that followed a sporotrichoid pattern. Histological study of nodular lesions showed a granulomatous dermatitis with numerous acid-fast bacilli. The mycobacterium was identified 3 months later by genetic hybridization from a cultive in solid medium. Combined therapy with isoniazid, rifampin, clarithromycin, ethambutol, amikacin and ciprofloxacin resulted in complete resolution of the lesions. Infection by Mycobacterium haemophilum is a rare mycobacteriosis that usually affects immunodepressed patients. The most common clinical manifestations are cutaneous lesions but the development of sporotrichoid nodular lymphangitis is exceptional


Subject(s)
Male , Adult , Humans , Acquired Immunodeficiency Syndrome/complications , AIDS-Related Opportunistic Infections/diagnosis , HIV Infections/complications , Mycobacterium Infections/diagnosis , Mycobacterium haemophilum/pathogenicity , Lymphangitis/diagnosis , Sporotrichosis/diagnosis , Anti-Bacterial Agents/therapeutic use
17.
Int J Oral Maxillofac Surg ; 32(3): 342-5, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12767886

ABSTRACT

Extraskeletal myxoid chondrosarcoma is a rare tumour affecting the head and neck. We present a new case located in the midfacial region. Clinical, pathological and therapeutical features are reviewed.


Subject(s)
Chondrosarcoma/pathology , Facial Neoplasms/pathology , Soft Tissue Neoplasms/pathology , Adult , Chondrosarcoma/surgery , Diagnosis, Differential , Facial Neoplasms/surgery , Female , Humans , Immunohistochemistry , S100 Proteins , Soft Tissue Neoplasms/surgery
18.
Trans R Soc Trop Med Hyg ; 94(6): 673-6, 2000.
Article in English | MEDLINE | ID: mdl-11198654

ABSTRACT

The efficacy of albendazole (ABZ) treatment for human neurocysticercosis (NCC) was assessed by using a monoclonal antibody-based parasite antigen detection ELISA which specifically detects the products of living cysticerci in human serum. The assay displayed 85% diagnostic sensitivity, detecting 39 of 46 NCC cases. Only patients with a single viable cyst or only enhancing lesions (degenerating parasites) were seronegative. Specificity of the assay was 92% (23/25) when tested in healthy Peruvian volunteers. In 'cured' patients, in whom all parasites died after ABZ therapy, parasite antigen levels fell sharply by 3 months post treatment. This pattern was not observed in patients refractory to treatment. The sensitivity of the assay with serum samples, and its ability to identify successfully treated patients, make this monoclonal antibody-based ELISA the test of choice for the follow-up of NCC cases.


Subject(s)
Antigens, Helminth/blood , Neurocysticercosis/diagnosis , Adolescent , Adult , Aged , Albendazole/therapeutic use , Anthelmintics/therapeutic use , Cohort Studies , Enzyme-Linked Immunosorbent Assay/standards , Female , Follow-Up Studies , Humans , Longitudinal Studies , Male , Middle Aged , Neurocysticercosis/drug therapy , Neurocysticercosis/epidemiology , Peru/epidemiology , Sensitivity and Specificity
19.
Trans R Soc Trop Med Hyg ; 92(4): 411-4, 1998.
Article in English | MEDLINE | ID: mdl-9850394

ABSTRACT

An enzyme-linked immunosorbent assay (ELISA) for the detection of antigen secreted by viable Taenia solium metacestodes (Ag-ELISA) was applied to 43 pre-treatment and 47 follow-up cerebrospinal fluid (CSF) samples from Peruvian patients with neurocysticercosis demonstrated by computed tomography and enzyme-linked immunoelectrotransfer blot assay. The sensitivity of the assay was 86%. Negative pre-treatment results in the Ag-ELISA test were restricted to patients with only a single live cyst or only enhancing lesions. Patients with hydrocephalus had higher levels of circulating antigen. There was no difference between antigen levels in CSF taken before and immediately after treatment (day 14). Levels of parasite antigen were significantly positively correlated with the number of live cysts detected by tomography and were also proportional to the number and intensity of antibody reactions recognized by the immunoblot diagnostic test. In contrast, there was a negative correlation with the number of enhancing lesions revealed by tomography, supporting the hypothesis that enhancing lesions correspond to a terminal, moribund stage of the parasite. The use of antigen-detection tests specific for viable metacestodes has immediate utility in the clinical context, not only providing important information on the viability of the parasites but also leading to an improved understanding of the pathogenesis of neurocysticercosis before and after drug treatment.


Subject(s)
Antigens, Helminth/isolation & purification , Enzyme-Linked Immunosorbent Assay/methods , Neurocysticercosis/diagnosis , Taenia/isolation & purification , Adult , Albendazole/therapeutic use , Animals , Anthelmintics/therapeutic use , Female , Humans , Hydrocephalus/parasitology , Male , Middle Aged , Neurocysticercosis/cerebrospinal fluid , Neurocysticercosis/drug therapy , Peru/epidemiology , Tomography, X-Ray Computed/methods
SELECTION OF CITATIONS
SEARCH DETAIL