RESUMO
We hypothesized that if infection is the proximate cause of congenital biliary atresia, an appropriate response to antigen would occur in lymph nodes contiguous with the biliary remnant. We compared the number of follicular germinal centers (GC) in 79 surgically excised hilar lymph nodes (LN) and 27 incidentally discovered cystic duct LNs in 84 subjects at the time of hepatic portoenterostomy (HPE) for biliary atresia (BA) to autopsy controls from the pancreaticobiliary region of non-septic infants >3 months old at death. All 27 control LN lacked GC, a sign in infants of a primary response to antigenic stimulation. GC were found in 53% of 106 LN in 56 of 84 subjects. Visible surgically excised LN contiguous with the most proximal biliary remnants had 1 or more well-formed reactive GC in only 26/51 subjects. Presence of GC and number of GC/LN was unrelated to age at onset of jaundice or to active fibroplasia in the biliary remnant but was related to older age at HPE. Absent GC in visible and incidentally removed cystic duct LNs predicted survival with the native liver at 2 and 3 years after HPE, P = .03, but significance was lost at longer intervals. The uncommon inflammatory lesions occasionally found in remnants could be secondary either to bile-induced injury or secondary infection established as obstruction evolves. The absence of consistent evidence of antigenic stimulation in LN contiguous with the biliary remnant supports existence of at least 1 major alternative to infection in the etiology of biliary atresia.
Assuntos
Atresia Biliar/patologia , Centro Germinativo/patologia , Fígado/patologia , Portoenterostomia Hepática , Fatores Etários , Atresia Biliar/diagnóstico , Atresia Biliar/etiologia , Atresia Biliar/cirurgia , Estudos de Casos e Controles , Feminino , Seguimentos , Humanos , Lactente , Recém-Nascido , Masculino , Resultado do TratamentoRESUMO
Acute cellular rejection remains a serious and frequent complication during the posttransplant course of small bowel allograft recipients. Currently, small bowel biopsies are the optimal method to identify this form of rejection. The morphological criteria for this diagnosis have been known for some time; however, no consensus study has classified these changes. To address issues in bowel transplant pathology, several pathologists experienced in this particular subdiscipline participated in a Pathology Workshop preceding the VIIIth International Small Bowel Transplant Symposium in Miami, Florida. Among the results of this workshop was the development a standardized grading scheme for acute cellular rejection in small bowel transplants.
Assuntos
Rejeição de Enxerto/patologia , Intestino Delgado/transplante , Transplante Homólogo/patologia , Biópsia , Diagnóstico Diferencial , Humanos , Intestino Delgado/patologia , Reprodutibilidade dos Testes , Transplante Homólogo/imunologiaAssuntos
Infecções por Adenoviridae/diagnóstico , Enterite/diagnóstico , Enterite/virologia , Rejeição de Enxerto/diagnóstico , Intestinos/transplante , Complicações Pós-Operatórias/diagnóstico , Transplante Homólogo/imunologia , Adenoviridae/isolamento & purificação , Diagnóstico Diferencial , Quimioterapia Combinada , Humanos , Imunossupressores/uso terapêutico , Complicações Pós-Operatórias/patologia , Estudos Retrospectivos , Transplante Homólogo/patologiaRESUMO
We report 2 neonatal deaths caused by cardiac tamponade related to peripherally inserted central catheters (PICCs). A total of 3 deaths were noted for 390 PICCs placed, giving an incidence of 0.76%. To determine the magnitude of neonatal death related to PICCs, directors of neonatal intensive care units in the United States were surveyed by means of a questionnaire. Myocardial perforation and pericardial effusion were reported by 29% and 43%, respectively. Deaths were attributed to PICCs by 24% of the respondents. Uniform guidelines need to be formulated to avoid this complication.
Assuntos
Tamponamento Cardíaco/etiologia , Cateterismo Venoso Central/efeitos adversos , Cateterismo Venoso Central/métodos , Evolução Fatal , Feminino , Humanos , Recém-Nascido , Unidades de Terapia Intensiva Neonatal , Masculino , Inquéritos e Questionários , Análise de SobrevidaAssuntos
Doença de Caroli , Cisto do Colédoco , Cirrose Hepática Biliar , Doença de Caroli/diagnóstico , Doença de Caroli/patologia , Doença de Caroli/cirurgia , Cisto do Colédoco/diagnóstico , Cisto do Colédoco/patologia , Cisto do Colédoco/cirurgia , Diagnóstico Diferencial , Humanos , Lactente , Fígado/patologia , Cirrose Hepática Biliar/diagnóstico , Cirrose Hepática Biliar/patologia , Cirrose Hepática Biliar/cirurgia , Transplante de Fígado , MasculinoRESUMO
Case history and necropsy findings of a 5-month-old infant with a unique heart defect with features of truncus arteriosus communis and aortopulmonary defect in combination with severe tricuspid stenosis are presented. There is a wide spectrum of remarkable heart defects between truncus arteriosus communis and aortopulmonary septal defect.
Assuntos
Defeito do Septo Aortopulmonar/patologia , Cardiopatias Congênitas/patologia , Estenose da Valva Tricúspide/patologia , Persistência do Tronco Arterial/patologia , Evolução Fatal , Humanos , Lactente , MasculinoRESUMO
Human sacral appendages have rarely been reported. We present a neonate with a thoracolumbar appendage resembling a penis, and discuss the nature of the anomaly and its diagnosis and management.
Assuntos
Coristoma , Pênis , Doenças da Medula Espinal , Coristoma/diagnóstico , Coristoma/etiologia , Coristoma/terapia , Humanos , Recém-Nascido , Masculino , Doenças da Medula Espinal/diagnóstico , Doenças da Medula Espinal/etiologia , Doenças da Medula Espinal/terapiaRESUMO
Idiopathic thrombotic thrombocytopenic purpura (TTP) is a thrombotic microangiopathy of obscure etiology. The fundamental pathologic lesion is a hyaline thrombus composed of platelets and some fibrin accompanied by endothelial cell proliferation and detachment, in the absence of an inflammatory response. We have previously demonstrated that plasmas from patients with both idiopathic TTP and a related disorder, sporadic hemolytic-uremic syndrome (HUS), induce apoptosis and expression of the apoptosis-associated molecule Fas (CD95) in vitro in those lineages of microvascular endothelial cells (MVECs) that are affected pathologically. We now demonstrate the presence of enhanced MVEC apoptosis in splenic tissues from patients with TTP, documented by terminal deoxynucleotidyl-transferase-mediated dUTP nick-end labeling (TUNEL) and morphology. This is accompanied by elevated Fas expression. It contrasts with the absence of apoptosis in splenic tissues obtained after splenectomy for trauma or immune thrombocytopenic purpura. TUNEL-positive cells, identified by immunohistochemistry as MVECs or macrophages, presumably engulfing apoptotic ECs, are noted in numerous areas, including those apart from microthrombi. Thus, it is unlikely that EC apoptosis is simply a sequela of thrombus formation. Based on these data, we propose that MVEC apoptosis is of pathophysiologic significance in idiopathic TTP/sporadic HUS.
Assuntos
Apoptose , Endotélio Vascular/patologia , Púrpura Trombocitopênica Trombótica/patologia , Baço/patologia , Adolescente , Adulto , Criança , Endotélio Vascular/imunologia , Feminino , Humanos , Marcação In Situ das Extremidades Cortadas , Masculino , Pessoa de Meia-Idade , Púrpura Trombocitopênica Trombótica/imunologia , Baço/irrigação sanguínea , Baço/imunologia , Receptor fas/imunologiaAssuntos
Neoplasias Laríngeas/patologia , Papiloma/patologia , Papillomaviridae , Infecções por Papillomavirus/patologia , Infecções Tumorais por Vírus/patologia , Criança , Pré-Escolar , DNA Viral/análise , Evolução Fatal , Feminino , Humanos , Hibridização In Situ , Neoplasias Laríngeas/complicações , Neoplasias Laríngeas/virologia , Leucemia Mielogênica Crônica BCR-ABL Positiva/complicações , Leucemia Mielogênica Crônica BCR-ABL Positiva/patologia , Neoplasias Pulmonares/complicações , Neoplasias Pulmonares/patologia , Neoplasias Pulmonares/virologia , Recidiva Local de Neoplasia/patologia , Papiloma/complicações , Papillomaviridae/isolamento & purificação , Reação em Cadeia da PolimeraseAssuntos
Coartação Aórtica/complicações , Neuroblastoma/complicações , Neoplasias Retroperitoneais/complicações , Coartação Aórtica/diagnóstico , Coartação Aórtica/patologia , Feminino , Humanos , Recém-Nascido , Masculino , Estadiamento de Neoplasias , Neuroblastoma/diagnóstico , Neuroblastoma/patologia , Neoplasias Retroperitoneais/diagnóstico , Neoplasias Retroperitoneais/patologia , Espaço Retroperitoneal/patologiaRESUMO
OBJECTIVES: Systemic lupus erythematosus and antiphospholipid antibody, often identified in patients with systemic lupus erythematosus, are associated with poor pregnancy outcome. This study distinguishes between the effect of each of these factors on gestational outcome and placental pathologic conditions in pregnant patients with systemic lupus erythematosus. STUDY DESIGN: Thirty-seven pregnancies and 40 placentas from 33 women with systemic lupus erythematosus were studied prospectively. RESULTS: Systemic lupus erythematosus alone, but not systemic lupus erythematosus activity, was associated with increased spontaneous abortions, preterm gestations, and fetal growth restriction. Placental correlates were ischemic-hypoxic change, decidual vasculopathy, decidual and fetal thrombi, chronic villitis, and decreased placental weight. Extensive infarction and fetal death were important antiphospholipid antibody-related findings. CONCLUSIONS: Decidual vasculopathy/coagulopathy appears to mediate the antiphospholipid antibody-related and much of the systemic lupus erythematosus-related deleterious effect on the placenta and gestational outcome. The presence of antiphospholipid antibody largely, but not invariably, predicts fetal death. Antiphospholipid antibody-independent chronic villitis may represent a second mechanism of systemic lupus erythematosus-related change.
Assuntos
Anticorpos Antifosfolipídeos/sangue , Lúpus Eritematoso Sistêmico/patologia , Placenta/patologia , Adulto , Feminino , Seguimentos , Humanos , Lúpus Eritematoso Sistêmico/imunologia , Gravidez , Resultado da Gravidez , Estudos Prospectivos , Fatores de RiscoRESUMO
We report two cases of desmoplastic small round cell tumor (DSRCT) with novel molecular variants of the specific EWS-WT1 gene fusion. This fusion usually encodes a chimeric RNA with an in-frame junction of exon 7 of EWS to exon 8 of WT1. In one variant patient, the EWS-WT1 fusion transcript contained an in-frame junction of exon 9 of EWS to exon 8 of WT1. Moreover, in this patient the tumor arose in the hand, an extremely unusual site for DSRCT. In the second patient, an in-frame junction of exon 10 of EWS to exon 8 of WT1 was present. These two cases of DSRCT show that the molecular variability in the EWS breakpoint observed in the EWS-FLI1 fusion of Ewing's sarcoma can occur in DSRCT as well. This type of heterogeneity is relevant to the interpretation of molecular diagnostic assays and could also affect the functional properties of the encoded chimeric transcription factors.
Assuntos
Neoplasias Ósseas/genética , Carcinoma de Células Pequenas/genética , Fibroma Desmoplásico/genética , Dedos , Proteínas de Fusão Oncogênica/genética , Neoplasias de Tecidos Moles/genética , Adolescente , Adulto , Neoplasias Ósseas/patologia , Carcinoma de Células Pequenas/patologia , Feminino , Fibroma Desmoplásico/patologia , Humanos , Masculino , Neoplasias de Tecidos Moles/patologia , Translocação GenéticaRESUMO
The mean mature spermatid count (MMSC) provides a useful, simplified quantitative evaluation of human spermatogenesis that is based on the number of mature spermatids in histological sections of testicular biopsies. Here, the activity of the acid-fast (AF) stain was compared to that of the usual hematoxylin and eosin (H&E) stain in performing the MMSC. Thirty bilateral testicular biopsies showing normal spermatogenesis were chosen retrospectively from 15 subfertile patients with obstructive azoospermia or severe oligospermia. The MMSC was determined on each biopsy by utilizing both H&E and AF stains. The AF stain proved to be specific for the mature spermatids normally counted for the MMSC. It simplified recognition of mature spermatids, thereby shortening the overall time required for the procedure. The mean AF MMSC was lower than the mean H&E MMSC, and the mean interobserver differences were decreased. The AF stain is a superior stain for the MMSC when used in conjunction with the H&E stain for descriptive histology.
Assuntos
Corantes/normas , Infertilidade Masculina/patologia , Contagem de Espermatozoides , Espermátides , Testículo/patologia , Adulto , Biópsia , Humanos , Concentração de Íons de Hidrogênio , Masculino , Pessoa de Meia-IdadeRESUMO
Byler disease (ByD) is an autosomal recessive disorder in which cholestasis of onset in infancy leads to hepatic fibrosis and death. Children who have a clinically similar disorder, but are not members of the Amish kindred in which ByD was described, are said to have Byler syndrome (ByS). Controversy exists as to whether ByD and ByS (subtypes of progressive familial intrahepatic cholestasis [PFIC]) represent one clinicopathological entity. The gene for ByD has been mapped to a 19-cM region of 18q21-q22. PFIC caused by a lesion in this region, including ByD, can be designated PFIC-1. Examination of haplotypes in siblings with ByS in two unrelated non-Amish families showed that the gene(s) responsible for their disorder(s) did not lie in the PFIC-1 candidate region. On light microscopy and transmission electron microscopy (TEM), liver tissue differed between Amish children with PFIC-1, who had coarsely granular bile and at presentation had bland intracanalicular cholestasis, and the children with ByS in the two non-Amish families, who had amorphous or finely filamentous bile and at presentation had neonatal hepatitis. Bile acid composition of bile also differed: In the Amish children with PFIC-1 and in one ByS family, the proportional concentration of chenodeoxycholic acid (CDCA) in bile was low compared with normal bile; in the other ByS family, it was only slightly reduced. Genetic analysis and light microscopy and TEM of liver may help distinguish PFIC-1 from other forms of ByS.
Assuntos
Colestase Intra-Hepática/genética , Colestase Intra-Hepática/patologia , Fígado/patologia , Bile/química , Biópsia , Humanos , Lactente , Recém-Nascido , Fígado/ultraestrutura , Microscopia Eletrônica , LinhagemRESUMO
Multiple foci of heterotopic liver in the jejunum were sequentially discovered in an infant boy at the ages of 1 day, 2 months, and 4 months. This is the second reported case of jejunal heterotopic liver, a rare entity in any site. Progressive histological changes indicative of biliary duct obstruction were observed in the hepatic heterotopias, which demonstrated no connections to the main body of the liver or biliary tree.
Assuntos
Coristoma/patologia , Doenças do Jejuno/patologia , Fígado , Atresia Biliar/patologia , Atresia Biliar/cirurgia , Progressão da Doença , Evolução Fatal , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Doenças do Jejuno/cirurgia , MasculinoRESUMO
We report a case of an infantile myofibromatosis with hemangiopericytoma-like features arising in the tongue of a 5-month-old female infant. Many authors now classify neoplasms as infantile myofibromatosis that were previously called infantile hemangiopericytoma. The ultrastructural features of our tumor illustrate its biphasic nature and provide a possible explanation for its histogenesis. Infantile myofibromatosis, including those diagnosed as infantile hemangiopericytomas, rarely arise in any intraoral location. Despite the generally good prognosis associated with these neoplasms, complete surgical excision is recommended to avoid recurrences.
Assuntos
Hemangiopericitoma/patologia , Hemangiopericitoma/ultraestrutura , Miofibromatose/patologia , Neoplasias da Língua/patologia , Neoplasias da Língua/ultraestrutura , Diagnóstico Diferencial , Feminino , Hemangiopericitoma/química , Humanos , Imuno-Histoquímica , Lactente , Miofibromatose/diagnóstico , Miofibromatose/metabolismo , Neoplasias da Língua/químicaRESUMO
Recent work has implicated nitric oxide (NO) in several aspects of male genital physiology including erectile function and androgen secretion, as well as in vitro effects on sperm motility and capacitation. The objectives of this study were to characterize the distribution of endothelial nitric oxide synthase (eNOS) in "normal" human testis, epididymis, and vas deferens and in testis pathology. Nitric oxide synthase protein was localized immunohistochemically using an eNOS monoclonal antibody. Endothelial NOS protein co-localized to areas that showed positive NADPH diaphorase activity. Within the testis, eNOS protein was localized to the cytoplasm of Leydig cells and Sertoli cells at all stages of spermatogenesis. Within the epididymis and vas deferens, eNOS was localized to the epithelium. Endothelial NOS was also localized to endothelial cells in all tissues; it was not detectable in normal germ cells. Endothelial NOS and diaphorase activity were, however, detected in degenerating or apoptotic intraepithelial germ cells. In addition, prematurely shed spermatocytes and spermatids had intense eNOS expression. Previous studies have suggested a role for NOS in the contractile, hemodynamic, and hormonal aspects of testicular function as well as in epididymal secretion. The studies reported herein suggest a role for eNOS in spermatogenesis and germ cell degeneration.
Assuntos
Epididimo/enzimologia , Óxido Nítrico Sintase/análise , Óxido Nítrico/fisiologia , Espermatozoides/fisiologia , Testículo/enzimologia , Ducto Deferente/enzimologia , Especificidade de Anticorpos , Apoptose , Western Blotting , Fragmentação do DNA , Humanos , Imuno-Histoquímica , Masculino , NADPH Desidrogenase/análise , EspermatogêneseRESUMO
The cellular expression of pituitary gonadotropin receptors in gonadal tissues is poorly defined because of the lack of suitable reagents. In this study, we developed in situ hybridization and reverse transcription polymerase chain reaction techniques for the evaluation of follicle-stimulating hormone receptor (FSHR) expression in the ovary and fallopian tube. Using a single-strand RNA probe, we demonstrated that FSHR mRNA expression is strongest in Graafian follicles. Within these developing follicles, granulosa cells showed the greatest expression, although both theca interna and theca externa were also positive, interna greater than externa. Granulosa cells in both primary and primordial follicles were positive, with primordial follicles showing only weak focal positivity. Ovarian surface epithelium and fallopian tube epithelium, not previously recognized to express FSHR, were both strongly positive. The FSHR expression in the ovary and fallopian tube was confirmed by reverse transcription polymerase chain reaction. Our results indicated that the FSHR is expressed in a cell-specific fashion at different stages of follicular development and is also expressed in ovarian surface and fallopian tube epithelia. The presence of FSHR in ovarian surface epithelium and of gonadotropin-binding sites in ovarian neoplasms provide additional evidence supporting the derivation of epithelial ovarian tumors from the surface epithelium and should promote heightened interest in the gonadotropin theory of ovarian tumorigenesis. More importantly, this study shows the feasibility of evaluating FSHR expression by both in situ hybridization and reverse transcription polymerase chain reaction. Application of these techniques to tumor specimens will help to elucidate the role of gonadotropins and their receptors in the carcinogenesis of gynecological tumors.
Assuntos
Tubas Uterinas/química , Ovário/química , RNA Mensageiro/análise , Receptores do FSH/análise , Sequência de Bases , Epitélio/química , Estudos de Viabilidade , Feminino , Humanos , Hibridização In Situ/métodos , Dados de Sequência Molecular , Folículo Ovariano/química , Reação em Cadeia da Polimerase/métodosRESUMO
OBJECTIVES: To describe the pulmonary pathology and clinical outcome in children with acute hypoxemic respiratory failure after bone marrow transplantation. DESIGN: Review of medical records and pathologic material of patients diagnosed with acute hypoxemic respiratory failure after bone marrow transplantation. SETTING: Pediatric intensive care unit (ICU) of a teaching hospital. PATIENTS AND METHODS: Retrospective review of a consecutive cohort of children, with a history of bone marrow transplantation admitted to the pediatric ICU during a 7-yr study period, and who met a published definition of acute hypoxemic respiratory failure. For each admission, the pediatric ICU course and outcome were reviewed. Pathologic material that was obtained from the patients was reexamined and assigned to one of the following categories: acute or organizing diffuse alveolar damage, pulmonary hemorrhage, nonspecific interstitial pneumonitis, or infectious pneumonia. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Forty-three patients satisfied criteria for inclusion in the study group. Indications for bone marrow transplantation were: solid tumor (30%), leukemia (44%), congenital immunodeficiency (19%), and aplastic anemia (7%). Patients were admitted to the pediatric ICU a median of 1 month (range 0 to 126) after bone marrow transplantation. Thirty-eight (88%) patients died in the pediatric ICU. Tissue histologic material was available from 21 (49%) patients. Six (29%) of 21 patients had acute diffuse alveolar damage; one (5%) had organizing diffuse alveolar damage; three (14%) had nonspecific interstitial pneumonitis; and two (10%) had pulmonary hemorrhage. Infectious pneumonia occurred in nine (43%) cases (five fungal; four viral). CONCLUSIONS: The acute mortality rate (88%) for children with acute hypoxemic respiratory failure after bone marrow transplantation is similar to that reported for adults with this combination of conditions. Diffuse alveolar damage, the histologic hallmark of adult respiratory distress syndrome, was present in a minority (33%) of patients. Infectious pneumonia was the most frequent cause of acute hypoxemic respiratory failure in patients who had pathologic tissue available, emphasizing the need for aggressive diagnostic studies and early institution of antifungal and antiviral therapy.
Assuntos
Transplante de Medula Óssea/efeitos adversos , Hipóxia/etiologia , Pulmão/patologia , Insuficiência Respiratória/etiologia , Doença Aguda , Adolescente , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Pneumopatias/etiologia , Pneumopatias/patologia , Masculino , Insuficiência Respiratória/patologia , Estudos RetrospectivosRESUMO
Familial arrhythmogenic right ventricular dysplasia is a rare cardiomyopathy that is usually diagnosed on postmortem examination or on presentation with progressive congestive heart failure. We present a patient in whom an automatic implantable cardioverter-defibrillator was inserted prophylactically. A review of the condition and possible therapies is included.