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1.
Am J Dermatopathol ; 33(2): 152-60, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21317613

RESUMO

BACKGROUND: Lymphangiectases are a histologic sign of lymphostasis, which is associated with decreased immune cell trafficking and cell-mediated immunity. OBJECTIVE: To determine if latent lymphedema is apparent underlying warts and in skin affected by cutaneous neoplasia. MATERIALS AND METHODS: The number and maximal dilation of lymphangiectases were measured in the upper half of the dermis of 51 consecutive biopsies of warts, 230 consecutive normal skin samples from primary skin tumor excisions, and 14 normal skin samples from breast reduction (11) and panniculectomy (3) specimens. RESULTS: All warts had one or more underlying lymphangiectases compared with 79% of peritumor normal skin samples and 50% of cosmetic specimens. The mean number of lymphangiectases and mean maximal dilation were significantly greater in warts than in peritumor skin, which was significantly greater than cosmetic skin samples (3.6 vs. 1.3 vs. 0.12 lymphangiectases per square millimeter and 54 vs. 23 vs. 1 µm, respectively; P = 0.0001). Warts exhibited mild fibrosis significantly more frequently than peritumor skin (57% vs. 5%; P = 0.0001). For peritumor (normal) skin, age, solar elastosis, and adjacent malignancy correlated with greater dilation of lymphatics. Solar elastosis also correlated with increased number of lymphangiectases. CONCLUSIONS: Minor trauma and solar elastosis from chronic ultraviolet radiation exposure are likely the etiologic factors in the development of lymphostasis. By decreasing immune surveillance, latent lymphedema ostensibly facilitates human papillomavirus infection and carcinogenesis.


Assuntos
Vigilância Imunológica/imunologia , Linfangiectasia/patologia , Dermatopatias/imunologia , Dermatopatias/patologia , Verrugas/imunologia , Verrugas/patologia , Adolescente , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Criança , Pré-Escolar , Feminino , Humanos , Linfangiectasia/imunologia , Masculino , Pessoa de Meia-Idade , Envelhecimento da Pele/imunologia , Envelhecimento da Pele/patologia , Neoplasias Cutâneas/patologia , Adulto Jovem
2.
Microsurgery ; 27(4): 339-45, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17477428

RESUMO

The authors report their experience in the diagnosis and treatment of lymphatic and chylous disorders in the thoracic and abdominal areas. Sixteen patients (10 adults, 6 children) affected by primary chylous ascites with associated syndromes and consequent immunological incompetence were studied. Diagnostic investigations included abdominal sonography scans, lymphoscintigraphy, and lymphography combined with computed tomography and laparoscopy. Surgical treatment included laparoscopy, drainage of ascites and/or the chylothorax, treatment of abdominal and retroperitoneal chylous leaks, exeresis of lymphodysplastic tissues, ligation of incompetent lymph vessels also by CO(2) LASER, and chylo-venous and lympho-venous microsurgical shunts. Eleven patients did not have a relapse of the ascites and four patients had a persistence of a small quantity of ascites with no protein imbalance. All patients had an improvement of their immunocompetence. Median follow-up was 5 years. We demonstrated that the use of microsurgery is remarkably advantageous for performing a causal treatment of the dysfunction.


Assuntos
Quilotórax/cirurgia , Ascite Quilosa/cirurgia , Linfangiectasia/cirurgia , Vasos Linfáticos/cirurgia , Veias Mesentéricas/cirurgia , Microcirurgia , Adulto , Anastomose Cirúrgica , Criança , Pré-Escolar , Quilotórax/imunologia , Ascite Quilosa/imunologia , Feminino , Seguimentos , Humanos , Lactente , Ligadura/métodos , Linfangiectasia/imunologia , Vasos Linfáticos/patologia , Linfografia , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Recidiva , Resultado do Tratamento
3.
J Allergy Clin Immunol ; 84(4 Pt 1): 515-20, 1989 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-2529303

RESUMO

Peripheral blood lymphocyte subsets were enumerated in five children with abnormal lymphatic circulation (three with lymphangiectasia, one with chylothorax, and one child with chyloperitoneum). All patients were lymphopenic. The percentage and absolute number of blood T-lymphocytes (CD3) were low in two children and normal in the other children. The percentage and absolute number of helper/inducer lymphocytes (CD4) were markedly reduced in all patients. The percentage of suppressor/cytotoxic lymphocytes (CD8) was normal or elevated in all children, and the absolute number of CD8 cells was normal in three patients. The CD4/CD8 ratio was reversed in all patients. In the two patients tested, the proliferative response of peripheral blood mononuclear cells to mitogens was reduced. T-lymphocyte subsets were measured in the pleural or peritoneal fluid of three patients, and the CD4/CD8 ratio was normal or increased. In each child, the CD4/CD8 ratio in the lymphatic fluids was markedly higher than the CD4/CD8 ratio of the blood (4.0/0.45, 1.75/0.95, and 1.3/0.85). The reversed CD4/CD8 ratio in the blood in cases of chronic loss of chyle may be due to either selective transport of CD4 lymphocytes into the lymphatic fluids or a shorter half-life of CD8 compared to CD4 lymphocytes. This finding may in part explain the abnormal cellular immunity previously observed in patients with lymphangiectasia.


Assuntos
Doenças Linfáticas/imunologia , Linfócitos T/imunologia , Adolescente , Antígenos de Diferenciação de Linfócitos T , Antígenos CD4/análise , Antígenos CD8 , Criança , Quilotórax/imunologia , Ascite Quilosa/imunologia , Humanos , Lactente , Contagem de Leucócitos , Linfangiectasia/imunologia , Linfócitos T Auxiliares-Indutores/imunologia , Linfócitos T Reguladores/imunologia
4.
Arch Dermatol ; 125(1): 92-7, 1989 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-2642686

RESUMO

The term penicillamine dermatopathy refers to the characteristic hemorrhagic skin lesions found in persons receiving long-term penicillamine therapy for either Wilson's disease or cystinuria. These lesions are thought to develop as a result of faulty collagen and elastin synthesis. We describe a patient with Wilson's disease who developed extensive penicillamine dermatopathy. In addition, histologic, immunochemical, and ultrastructural studies revealed multiple lymphangiectases with blood vessel to lymphatic anastomosis within these lesions, a finding not previously reported. The possible relationship to defective collagen and elastin formation are considered.


Assuntos
Degeneração Hepatolenticular/tratamento farmacológico , Linfangiectasia/induzido quimicamente , Penicilamina/efeitos adversos , Dermatopatias/induzido quimicamente , Adulto , Biópsia , Colágeno/biossíntese , Tecido Conjuntivo/ultraestrutura , Elastina/biossíntese , Humanos , Técnicas Imunoenzimáticas , Linfangiectasia/imunologia , Linfangiectasia/patologia , Masculino , Microscopia Eletrônica/métodos , Penicilamina/uso terapêutico , Pele/imunologia , Pele/ultraestrutura , Dermatopatias/metabolismo , Dermatopatias/patologia
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