RESUMO
Squamous metaplasia in the skin has been reported in the eccrine ducts as eccrine squamous syringometaplasia (ESS). To our knowledge, squamous metaplasia of sebaceous gland (SMSG) has not been described in human skin. Twenty-two biopsy specimens from patients with pressure lesions after cardiac surgery with extracorporeal circulation were evaluated for the presence of SMSG. Squamous metaplasia of sebaceous gland was identified in five of the eight scalp biopsies and none of the buttock biopsies. The squamous metaplasia began in the germinative outer layer and advanced in a centripetal way. We believe that SMSG is an unspecific change of the sebaceous cells secondary to a chronic injury. Ischemia appears to play a mayor role, but other factors such as chronic trauma or toxicosis can not be ruled out.
Assuntos
Glândulas Sebáceas/patologia , Carcinoma de Células Escamosas/patologia , Epitélio/patologia , Humanos , Metaplasia/patologia , Neoplasias das Glândulas Sebáceas/patologiaAssuntos
Infecções Oportunistas Relacionadas com a AIDS/complicações , Infecções por Citomegalovirus/complicações , Doenças das Glândulas Sudoríparas/complicações , Adulto , Infecções por Citomegalovirus/virologia , Glândulas Écrinas/patologia , Glândulas Écrinas/virologia , Células Epiteliais/patologia , Células Epiteliais/virologia , Feminino , Humanos , Masculino , Metaplasia , Doenças das Glândulas Sudoríparas/virologiaRESUMO
The term HIV-associated eosinophilic folliculitis (EF) designates an idiopathic dermatitis that appears in HIV-infected patients with different clinical manifestations but with a distinctive histological feature characterized by a predominantly eosinophilic infiltrate in the follicular infundibula. On the other side, follicular mucinosis (FM) is a reaction pattern in the follicular epithelium, characterized by a mucinous degeneration of the outer sheath of follicles and sebaceous glands. It has been described in association with a variety of unrelated conditions. We report 2 HIV-infected patients with a pruritic papular eruption. Histopathological study revealed the coexistence of EF and FM. To our knowledge, this is the first report that describes this association. The possible relationship between these two entities is discussed.
Assuntos
Eosinofilia/complicações , Foliculite/complicações , Infecções por HIV/complicações , Mucinose Folicular/complicações , Adulto , Eosinofilia/patologia , Eosinofilia/virologia , Foliculite/patologia , Foliculite/virologia , Homossexualidade Masculina , Humanos , Masculino , Mucinose Folicular/patologia , Mucinose Folicular/virologia , Pele/patologia , Pele/virologiaRESUMO
In the epidermis, beta1 integrin expression is normally confined to the basal layer; however, suprabasal expression of beta1 integrins in keratinocytes has been found in psoriasis, and it has been suggested that it could be a pathogenic factor of the disease. We have investigated herein the functional state of beta1 integrins of human keratinocytes in normal skin and psoriasis. The expression of beta1-activation-reporter epitopes was monitored with two monoclonal antibodies, HUTS-21 and MG5A7, that recognize epitopes whose expression parallels functional activity of beta1 integrins and correlates with the ligand binding activity of these heterodimeric glycoproteins. We have found that keratinocytes express activation epitopes of beta1 integrins, and that these epitopes can be modulated by manganese. The expression of activation epitopes of beta1 integrins was related to an enhanced adhesion to fibronectin and collagen. Immunohistochemical studies of normal and psoriatic skin with HUTS-21 and other monoclonal antibodies indicate that, although there is suprabasal expression of beta1 integrins in psoriasis, these molecules seem to be in an inactive state. Moreover, most beta1 integrins in lateral and apical surfaces of basal keratinocytes of psoriasis are also in a nonactive conformation, implying a decrease of activity compared with normal skin, in which active beta1 integrins are distributed all over the basal keratinocytes.
Assuntos
Integrina beta1/análise , Psoríase/metabolismo , Pele/química , Células Cultivadas , Epitopos , Humanos , Queratinócitos/químicaRESUMO
Metaplastic synovial cyst is a recently reorganized entity characterized by a cystic space lined by polygonal cells and villous structures resembling synovium pointing toward the lumen. It usually develops following trauma. We report a 15-year-old girl with Ehlers-Danlos syndrome who developed a nodular lesion of her elbow without previous trauma. Histopathological and immunohistochemical studies yielded results similar to those reported in cases of cutaneous metaplastic synovial cyst. This case appears to be the first one reported of cutaneous metaplastic synovial cyst associated with an Ehlers-Danlos syndrome. Cutaneous fragility and anomalous scarring typical of Ehlers-Danlos syndrome may be related to the development of this pseudocyst. If so, other connective-tissue diseases with increased skin fragility could be susceptible to development of such lesions.
Assuntos
Síndrome de Ehlers-Danlos/patologia , Cotovelo/patologia , Dermatopatias/patologia , Cisto Sinovial/patologia , Adolescente , Cicatriz/patologia , Doenças do Tecido Conjuntivo/patologia , Citoplasma/ultraestrutura , Suscetibilidade a Doenças , Feminino , Humanos , Técnicas Imunoenzimáticas , Metaplasia , Estresse Mecânico , Vimentina/análiseAssuntos
Antirreumáticos/efeitos adversos , Autoanticorpos/análise , Moléculas de Adesão Celular/imunologia , Proteínas do Citoesqueleto/imunologia , Doença Mista do Tecido Conjuntivo/tratamento farmacológico , Pênfigo/induzido quimicamente , Penicilamina/efeitos adversos , Adulto , Antirreumáticos/uso terapêutico , Desmogleína 1 , Desmogleínas , Desmoplaquinas , Feminino , Humanos , Pênfigo/imunologia , Penicilamina/uso terapêuticoAssuntos
Antimetabólitos Antineoplásicos/efeitos adversos , Eritema/induzido quimicamente , Dermatoses do Pé/induzido quimicamente , Dermatoses da Mão/induzido quimicamente , Hiperpigmentação/induzido quimicamente , Doenças da Unha/induzido quimicamente , Parestesia/induzido quimicamente , Tegafur/efeitos adversos , Doenças da Língua/induzido quimicamente , Adenocarcinoma/tratamento farmacológico , Adenocarcinoma/secundário , Feminino , Humanos , Ceratodermia Palmar e Plantar/etiologia , Neoplasias Hepáticas/tratamento farmacológico , Neoplasias Hepáticas/secundário , Pessoa de Meia-Idade , Neoplasias Gástricas/patologiaRESUMO
BACKGROUND AND OBJECTIVE: Papular-purpuric gloves-and-socks syndrome (PPGSS) is a recently described dermatosis in which human parvovirus B19 (HPV B19) has been implicated as etiologic agent; however, it is suspected that PPGSS may be caused by various agents. This study was designed to survey the general characteristics of PPGSS and to determine the role of HPV B19 in its etiology. METHODS: We analyzed data from 21 patient and examined serum samples from three new cases for various viruses. RESULTS: The PPGSS displays a striking uniform clinical pattern. Histologic and immunofluorescence findings are non-specific. Seroconversion of HPV B19 was reported in six cases and confirmed in two of our patients. In only one case was a possible causative role of Coxsackie virus B6 suggested consistently. CONCLUSIONS: The PPGSS represents a distinctive dermatosis and a manifestation of HPV B19 infection. Unlike erythema infectiosum, anti-HPV B19 antibodies seem to develop later after onset of the skin eruption and while viremia is still present.
Assuntos
Anticorpos Antivirais/análise , Eritema Infeccioso/diagnóstico , Dermatoses do Pé/diagnóstico , Dermatoses da Mão/diagnóstico , Parvovirus B19 Humano/imunologia , Adolescente , Adulto , Criança , Ensaio de Imunoadsorção Enzimática , Eritema Infeccioso/fisiopatologia , Feminino , Dermatoses do Pé/etiologia , Dermatoses do Pé/virologia , Dermatoses da Mão/etiologia , Dermatoses da Mão/virologia , Humanos , Masculino , Remissão EspontâneaRESUMO
Diffuse plane normolipaemic xanthomatosis (DPNX) is a well-defined clinicopathological entity that characteristically presents with yellow-orange plaques in the periorbital areas, the neck, the upper trunk and the flexural folds. DPNX has been reported in association with lymphoproliferative disorders and, occasionally, with miscellaneous, probably coincidental disorders. A case of DPNX in a patient with an IgG lambda monoclonal gammopathy and systemic amyloidosis is reported. Clinical and histopathological findings revealed typical features of DPNX and amyloidosis coexisting in the cutaneous lesions. To our knowledge this is the first reported case showing coexistence of xanthoma and amyloidosis in cutaneous lesions in a patient with a monoclonal gammopathy.
Assuntos
Amiloidose/complicações , Paraproteinemias/complicações , Xantomatose/complicações , Idoso , Idoso de 80 Anos ou mais , Amiloidose/patologia , Feminino , Humanos , Imunoglobulina G/sangue , Xantomatose/patologiaAssuntos
Infecções Oportunistas Relacionadas com a AIDS/parasitologia , Soropositividade para HIV/patologia , Escabiose/patologia , Vasculite Leucocitoclástica Cutânea/parasitologia , Infecções Oportunistas Relacionadas com a AIDS/patologia , Adulto , Animais , Humanos , Masculino , Sarcoptes scabiei , Vasculite Leucocitoclástica Cutânea/patologiaRESUMO
Idiopathic plantar hidradenitis (IPH) is a recently described condition primarily affecting healthy children who develop tender lesions localized to the plantar or lateral aspects of the feet with histologic findings similar to those seen in neutrophilic eccrine hidradenitis (NEH), although with certain notable exceptions including the absence of syringosquamous metaplasia and the presence, in most cases, of neutrophilic abscesses adjacent to eccrine coils. Since its original description, three additional patients have been reported, one with palmoplantar lesions, extending the disease's clinical spectrum to include palmar as well as plantar surfaces. We report on a healthy 8-year-old girl with tender, erythematous nodules on palms and soles and review the literature on this subject.
Assuntos
Dermatoses do Pé/patologia , Dermatoses da Mão/patologia , Hidradenite/patologia , Abscesso , Criança , Feminino , Humanos , Neutrófilos/patologiaRESUMO
Although cases of lichen planus (LP) associated with hepatitis C virus (HCV) infection have been described, the association between the two diseases has not been established because the geographic origin of patients could be an important factor in HCV prevalence in patients with LP. The serum samples of 78 consecutive patients with cutaneous and/or mucous LP and 82 control patients were analysed for the presence of antibodies to HCV by enzyme-immunoassay and for the presence of antigens of HCV by two-stage polymerase chain reaction (PCR). The clinical features of patients with LP associated with HCV infection were compared with patients with LP without HCV infection. Sixteen of the 78 (20%) patients had anti-HCV antibodies. In 13 of these 16 cases (81%), HCV-RNA was detected by PCR in serum samples. In the 82 control patients, anti-HCV antibodies was observed in two (2.4%) patients. We have found a statistically significant association (P < 0.05) between erosive LP and HCV infection. We conclude that the high prevalence of HCV-RNA in patients with LP provides some evidence for the role of HCV in the pathogenesis of LP. Our results suggest an association between erosive LP and HCV infection.
Assuntos
Hepatite C/complicações , Líquen Plano/complicações , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos de Casos e Controles , Doença Crônica , Feminino , Hepacivirus/isolamento & purificação , Anticorpos Anti-Hepatite C/sangue , Humanos , Líquen Plano/virologia , Líquen Plano Bucal/virologia , Masculino , Pessoa de Meia-Idade , RNA Viral/sangue , Fatores de RiscoAssuntos
Infecções Oportunistas Relacionadas com a AIDS , Leishmaniose Cutânea/etiologia , Leishmaniose Visceral/complicações , Infecções Oportunistas Relacionadas com a AIDS/diagnóstico , Infecções Oportunistas Relacionadas com a AIDS/parasitologia , Adulto , Criança , Humanos , Leishmaniose Cutânea/diagnóstico , Leishmaniose Cutânea/patologia , Leishmaniose Visceral/diagnóstico , Leishmaniose Visceral/parasitologiaRESUMO
BACKGROUND: Mixed cryoglobulinemia (MC) is a systemic disorder, characterized by a typical clinical triad: purpura, weakness, and arthralgias, with visceral complications such as liver and renal involvement. The objective was to study the association between hepatitis C virus (HCV) infection and essential mixed cryoglobulinemia (EMC). PATIENTS AND METHODS: Markers of HCV infection in 11 patients with cryoglobulinemia were examined and hepatitis C virus (HCV) was detected in eight of them. These patients were included in a clinical and histologic study. Anti-HCV antibodies were determined by a second-generation enzyme-linked immunosorbent assay (ELISA-2) in sera and cryoprecipitates. Studies on HCV-RNA were performed by a two-stage polymerase chain reaction (PCR) in the serum. A control group, consisting of 28 patients with other cutaneous disorders, was studied for HCV infection using ELISA-2 and PCR. RESULTS: All patients had liver dysfunction, arthralgias, and purpura. Three patients had involvement of the peripheral nervous system, two had renal involvement, and one patient had Sjögren's syndrome. Cryocrits ranged from 3% to 20%. Six patients had type III cryoglobulinemia and the remaining two had type II. Markers for hepatitis B virus (HBV) were negative in all serum samples. Anti-HCV antibodies and HCV-RNA were positive in the serum of all the cases with MC. Anti-HCV antibodies were positive in all cases except for one of the cryoprecipitates tested. Four patients received recombinant interferon alfa. In two of them, serum aminotransferases became normal and cryoglobulins disappeared. CONCLUSIONS: The results strongly suggest that HCV infection is responsible for the cryoglobulinemia and vasculitis in patients with MC and that treatment with interferon alfa is presently the treatment of choice for such patients.
Assuntos
Crioglobulinemia/virologia , Hepatite C , Dermatopatias Vasculares/virologia , Vasculite Leucocitoclástica Cutânea/virologia , Adulto , Anticorpos Antivirais/análise , Anticorpos Antivirais/sangue , Artralgia/virologia , Crioglobulinas/análise , Ensaio de Imunoadsorção Enzimática , Feminino , Hepacivirus/genética , Hepacivirus/imunologia , Hepacivirus/isolamento & purificação , Hepatite C/terapia , Humanos , Interferon-alfa/uso terapêutico , Fígado/enzimologia , Fígado/fisiopatologia , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Púrpura/virologia , RNA Viral/análise , Transaminases/sangueRESUMO
We report the case of a 56-year-old woman with reticular erythematous mucinosis (REM). During her workup infection with the human immunodeficiency virus (HIV) was detected. She developed a cerebral toxoplasmosis, salmonella sp. bacteremia and oral ulcerations with the presence of type I herpes simplex virus and cytomegalovirus. The relation of REM with the deposition of mucin in AIDS patients' bone marrow and HIV infection is discussed. To our knowledge, this is the first report where REM is associated with HIV disease.