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1.
Ultrastruct Pathol ; 36(1): 23-30, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22292734

RESUMEN

Three cases of adamantinoma were studied by electron microscopy and immunohistochemistry. In the tubular pattern, well-differentiated epithelial cells and glandular structures were present, in addition to ill-defined glands. In the basaloid pattern, less differentiated epithelial cells with discohesion were seen in the central epithelial masses. This study established the epithelial nature of some tubular structures with slit-like lumina, easily misinterpreted as capillaries by light microscopy. Results also showed that the irregular spaces observed within the basaloid pattern probably result from cell discohesion. Moreover, this investigation demonstrates the epithelial nature of a subset of spindle cells within the stroma of adamantinoma and offers ultrastructural evidence for a probable mesenchymal-epithelial transformation as its histogenesis.


Asunto(s)
Adamantinoma/ultraestructura , Tibia/ultraestructura , Adamantinoma/metabolismo , Adulto , Diferenciación Celular , Células Epiteliales/metabolismo , Células Epiteliales/ultraestructura , Femenino , Humanos , Inmunohistoquímica , Masculino , Mesodermo/metabolismo , Mesodermo/ultraestructura , Metaplasia , Microscopía Electrónica de Transmisión , Persona de Mediana Edad
2.
Fetal Pediatr Pathol ; 30(1): 32-9, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21204664

RESUMEN

Sialoblastoma is the most common epithelial tumor of the salivary gland. We report a case of congenital sialoblastoma arising in a minor salivary gland of the buccal mucosa of a male infant. After radiologic evaluation, an incisional biopsy was performed and then the mass was excised en bloc. Histologic features were both favorable and unfavorable. However, there was no recurrence for 5 months. In spite of a reported histologic grading system, the clinical course of isolated sialoblastoma is considered unpredictable. More published case reports of this rare tumor may enable histologic and clinical correlation in order to accurately predict prognosis.


Asunto(s)
Neoplasias Glandulares y Epiteliales/patología , Neoplasias de las Glándulas Salivales/patología , Glándulas Salivales Menores/patología , Mejilla/patología , Supervivencia sin Enfermedad , Humanos , Recién Nacido , Imagen por Resonancia Magnética , Masculino , Mucosa Bucal/patología , Neoplasias Glandulares y Epiteliales/congénito , Neoplasias Glandulares y Epiteliales/cirugía , Pronóstico , Neoplasias de las Glándulas Salivales/congénito , Neoplasias de las Glándulas Salivales/cirugía , Resultado del Tratamiento
3.
J Surg Res ; 159(2): 611-7, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20097372

RESUMEN

BACKGROUND: Hepatic fibrosis leading to cirrhosis is the major morbidity in patients with biliary atresia (BA). This fibrosis is due to an imbalance in extracellular matrix (ECM) breakdown and deposition. We have previously demonstrated increased mRNA expression for inhibitors of ECM breakdown without increased expression for mediators of ECM deposition in our animal model of BA by d 14. However, only a mild degree of hepatic fibrosis was seen at this time. We hypothesized that expression patterns for these proteins may change once more significant fibrosis had been established, and added resuscitation to the model to improve survival. Interestingly, we found that some mice spontaneously recovered at later time points with resuscitation, and thus compared expression for inhibitors of ECM breakdown and deposition in sick and recovered mice to determine the differences. METHODS: Newborn Balb/c mice received an intraperitoneal injection 1.0 x 10(6) fluorescence forming units of rhesus rotavirus 24h after birth. Mice were monitored daily for weight gain, development of jaundice, acholic stools, and bilirubinuria. Fifty muL/g of 5% dextrose in normal saline were subcutaneously injected daily to each mouse starting on d 7 until sacrifice. Mice that survived past d 14 were sacrificed at d 21 after saline or RRV infection. Livers were then harvested post-injection d 21 for histologic and immunohistochemical analysis. RNA expression of known mediators of fibrosis was evaluated using quantitative real-time PCR. Protein expression was assessed using ELISA. Weights and normally distributed data were compared using Student's t test. Histologic findings were compared using Fisher's exact test. Comparisons of gene expression and skewed data were performed by the Mann-Whitney U test. Statistical significance was assigned to any P value less than 0.05. RESULTS: Daily resuscitation resulted in a 35% (24/68) survival rate to d 21 in our model. Mice that recovered were significantly heavier than those that remained ill on d 14 (6.15 +/- 1.16 versus 4.94 +/- 0.82, P = 0.02) and 21 (7.31 +/- 1.41 versus 4.14 +/- 0.53, P < 0.001) despite the fact that there was no difference between the groups with respect to weight on d 7 (4.29 +/- 0.90 versus 3.89 +/- 0.81, P = 0.32). We found that all (10/10) animals that displayed clinical signs of biliary atresia on d 21 had moderate or severe histologic findings, while only one (1/9) of the recovered animals had liver abnormalities at sacrifice (P < 0.001 versus sick group). We also found that the sick mice had statistically significant median fold-increases of mRNA expression for TIMP-1 (31.9 versus 9.1, P = 0.041), TIMP-4 (88.1 versus 1.8, P = 0.022), and MMP-7 (51.8 versus 11.9, P = 0.006) compared with those that recovered. There was a trend toward decreased mRNA expression for PAI-1, which did not reach statistical significance (median 27.7 versus 2.19, P = 0.066). Increased protein expression for TIMP-1 and PAI-1 were also found in the sick group. The mRNA expression for the fibrillar collagens, fibronectin-1, connective tissue growth factor, snail-1, TIMP-2 and -3, and MMP-2 and MMP-9 was not different in the sick and recovered groups 21 d after RRV infection, and was not elevated from baseline gene expression. CONCLUSIONS: With resuscitation added to the animal model of BA, some mice spontaneously recover while others progress to more significant hepatic fibrosis. Mice with hepatic fibrosis have a continued increase in mRNA expression of TIMP-1, TIMP-4, and MMP-7, with a trend toward increased mRNA expression of PAI-1 on d 21. Protein levels for TIMP-1 and PAI-1 were also increased in the sick mice. Recovered mice display mild to no hepatic parenchymal disease and a normal pattern of mRNA expression for the mediators of fibrosis tested. No increase in mRNA expression for the mediators of ECM deposition was found in either group. These data further support the notion that inhibition of ECM breakdown alone is sufficient to induce hepatic fibrosis. Modulation of this process may be a putative target for preventing liver injury in patients with BA.


Asunto(s)
Atresia Biliar/genética , Cirrosis Hepática/genética , Animales , Animales Recién Nacidos , Atresia Biliar/complicaciones , Atresia Biliar/patología , Atresia Biliar/virología , Ensayo de Inmunoadsorción Enzimática , Factores Eucarióticos de Iniciación/genética , Regulación de la Expresión Génica , Cirrosis Hepática/complicaciones , Cirrosis Hepática/patología , Cirrosis Hepática/virología , Ratones , Ratones Endogámicos BALB C , Inhibidor 1 de Activador Plasminogénico/genética , ARN Mensajero/genética , Remisión Espontánea , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Rotavirus , Infecciones por Rotavirus/complicaciones , Infecciones por Rotavirus/genética , Inhibidor Tisular de Metaloproteinasa-1/genética
4.
N Engl J Med ; 355(8): 788-98, 2006 Aug 24.
Artículo en Inglés | MEDLINE | ID: mdl-16928994

RESUMEN

BACKGROUND: The Loeys-Dietz syndrome is a recently described autosomal dominant aortic-aneurysm syndrome with widespread systemic involvement. The disease is characterized by the triad of arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate and is caused by heterozygous mutations in the genes encoding transforming growth factor beta receptors 1 and 2 (TGFBR1 and TGFBR2, respectively). METHODS: We undertook the clinical and molecular characterization of 52 affected families. Forty probands presented with typical manifestations of the Loeys-Dietz syndrome. In view of the phenotypic overlap between this syndrome and vascular Ehlers-Danlos syndrome, we screened an additional cohort of 40 patients who had vascular Ehlers-Danlos syndrome without the characteristic type III collagen abnormalities or the craniofacial features of the Loeys-Dietz syndrome. RESULTS: We found a mutation in TGFBR1 or TGFBR2 in all probands with typical Loeys-Dietz syndrome (type I) and in 12 probands presenting with vascular Ehlers-Danlos syndrome (Loeys-Dietz syndrome type II). The natural history of both types was characterized by aggressive arterial aneurysms (mean age at death, 26.0 years) and a high incidence of pregnancy-related complications (in 6 of 12 women). Patients with Loeys-Dietz syndrome type I, as compared with those with type II, underwent cardiovascular surgery earlier (mean age, 16.9 years vs. 26.9 years) and died earlier (22.6 years vs. 31.8 years). There were 59 vascular surgeries in the cohort, with one death during the procedure. This low rate of intraoperative mortality distinguishes the Loeys-Dietz syndrome from vascular Ehlers-Danlos syndrome. CONCLUSIONS: Mutations in either TGFBR1 or TGFBR2 predispose patients to aggressive and widespread vascular disease. The severity of the clinical presentation is predictive of the outcome. Genotyping of patients presenting with symptoms like those of vascular Ehlers-Danlos syndrome may be used to guide therapy, including the use and timing of prophylactic vascular surgery.


Asunto(s)
Anomalías Múltiples/genética , Receptores de Activinas Tipo I/genética , Aneurisma de la Aorta/genética , Anomalías Craneofaciales/genética , Mutación Missense , Receptores de Factores de Crecimiento Transformadores beta/genética , Anomalías Múltiples/mortalidad , Anomalías Múltiples/terapia , Adulto , Disección Aórtica/genética , Arterias/anomalías , Colágeno Tipo III/biosíntesis , Análisis Mutacional de ADN , Síndrome de Ehlers-Danlos/genética , Femenino , Mutación de Línea Germinal , Humanos , Masculino , Fenotipo , Embarazo , Complicaciones del Embarazo/genética , Proteínas Serina-Treonina Quinasas , Receptor Tipo I de Factor de Crecimiento Transformador beta , Receptor Tipo II de Factor de Crecimiento Transformador beta , Análisis de Supervivencia , Síndrome
5.
J Surg Res ; 154(1): 21-9, 2009 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-19084240

RESUMEN

INTRODUCTION: Biliary atresia (BA) is a progressive obliteration of the extrahepatic bile ducts resulting in hepatic fibrosis. The underlying mechanisms have not been defined. We used an animal model of BA to evaluate mediators of extracellular matrix (ECM) processing to determine which factors may be involved. METHODS: Newborn BALB/c mice received an intraperitoneal injection with rhesus rotavirus or saline within 24 h of birth. Livers were harvested on days 7 and 14 for histology and immunohistochemistry (IHC). RNA expression was determined using quantitative real-time PCR. Human liver from patients with BA and those having a resection for nonfibrosing diseases was also evaluated. RESULTS: In experimental mice, mRNA expression for tissue inhibitor of metalloproteinase (TIMP)-1 and matrix metalloproteinase (MMP)-7 was increased 18-fold and 69-fold, respectively on day 7, with further increases on day 14. On day 14, mRNA expression for plasminogen activator inhibitor (PAI)-1 (38-fold), TIMP-4 (9.5-fold), and MMP-9 (5.5-fold) mRNA was also observed. Furthermore, integrin alpha(v) beta(6) mRNA expression was increased on days 7 (11-fold) and 14 (6-fold). Presence of integrin alpha(v) beta(6) protein was confirmed by IHC in both mouse and human specimens in the proliferating biliary epithelium. CONCLUSIONS: Our data suggest experimental BA is associated with increased mRNA expression of ECM degradation inhibitors, TIMP-1, PAI-1, and TIMP-4. MMP-7 and MMP-9 expression is also elevated in this model. Furthermore, increased gene expression of integrin alpha(v)beta(6) was demonstrated and IHC confirmed protein expression. Integrin alpha(v)beta(6) or the inhibitors of ECM breakdown may be attractive targets for future treatment strategies.


Asunto(s)
Antígenos de Neoplasias/genética , Atresia Biliar/patología , Matriz Extracelular/patología , Integrinas/genética , Animales , Animales Recién Nacidos , Atresia Biliar/enzimología , Atresia Biliar/genética , Atresia Biliar/virología , Modelos Animales de Enfermedad , Inmunohistoquímica , Metaloproteinasa 7 de la Matriz/genética , Ratones , Ratones Endogámicos BALB C , ARN Mensajero/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Inhibidor Tisular de Metaloproteinasa-1/genética , Regulación hacia Arriba
6.
Lymphat Res Biol ; 6(1): 39-44, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18361769

RESUMEN

Consanguinity allows for the expression of rare genetic disorders. We present the first case of an infant, born to consanguineous parents, with congenital lamellar ichthyosis, congenital lymphatic malformation, congenital hypothyroidism, bilateral megaureter, benign external hydrocephalus, and syrinx of the spinal cord. We review the disorders, examine their genetic causes, and explore the genetic connection among them.


Asunto(s)
Anomalías Múltiples , Ictiosis Lamelar/complicaciones , Anomalías Linfáticas/patología , Anomalías Múltiples/patología , Anomalías Múltiples/cirugía , Axila/patología , Axila/cirugía , Hipotiroidismo Congénito/complicaciones , Consanguinidad , Humanos , Hidrocefalia/complicaciones , Lactante , Anomalías Linfáticas/complicaciones , Anomalías Linfáticas/cirugía , Masculino , Mutación , Complicaciones Posoperatorias , Infecciones por Pseudomonas , Infecciones Estafilocócicas , Siringomielia/complicaciones , Siringomielia/congénito , Pared Torácica/patología , Pared Torácica/cirugía , Transglutaminasas/genética , Enfermedades Ureterales/complicaciones , Enfermedades Ureterales/congénito
7.
Hum Pathol ; 38(12): 1772-8, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17714760

RESUMEN

Congenital cystic airway malformation/congenital pulmonary airway malformation (CCAM/CPAM) of the lung is a rare but well-described malformative lesion of pulmonary parenchyma characterized by the abnormal maturation of airways along with an increase in terminal respiratory structures, resulting in cysts of variable sizes. Five types have been classified based on morphological analysis. Although the etiology of the lesion is still unclear, recent data suggest that bronchial atresia is a predisposing/associated anomaly. A described association between type 1 CCAM/CPAM and bronchioloalveolar carcinoma suggests that type 1 CCAM/CPAM may predispose to malignant transformation by as yet unidentified tumorigenic mechanisms. Here we studied epidermal growth factor receptor (EGFR) and K-RAS oncogene, 2 biological markers closely associated with tumorigenesis and altered in many types of tumors, including lung carcinomas. For this purpose, we used immunohistochemistry and gene sequencing in paraffin-embedded tissue. Our results demonstrate expression of EGFR in types 1 and 3 CCAM/CPAM, with a distinctive distribution and intensity, compared with that of type 2. Of special interest, mucinous areas in 2 cases of type 1 CCAM/CPAM lacked EGFR expression, whereas adjacent epithelial cystic linings were strongly positive. This supports the hypothesis that mucinous differentiation in CCAM/CPAM, always present in cases with malignant transformation, could be related to other molecular pathways. The K-RAS gene was screened for mutations usually found in lung carcinomas; however, no mutations were present in any of the studied samples. These findings support the notion that EGFR may play an important role in the pathogenesis and phenotype of CCAM/CPAM.


Asunto(s)
Biomarcadores/análisis , Receptores ErbB/biosíntesis , Genes ras/genética , Anomalías del Sistema Respiratorio/genética , Anomalías del Sistema Respiratorio/metabolismo , Adenocarcinoma Bronquioloalveolar/genética , Adenocarcinoma Bronquioloalveolar/metabolismo , Niño , Preescolar , Quistes/genética , Quistes/metabolismo , Feto , Expresión Génica , Humanos , Inmunohistoquímica , Lactante , Recién Nacido , Neoplasias Pulmonares/genética , Neoplasias Pulmonares/metabolismo , Mutación , Reacción en Cadena de la Polimerasa
8.
Hum Pathol ; 38(8): 1184-91, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17509661

RESUMEN

Activation of intracellular mitogenic signal transduction pathways driven by the ErbB family of receptor tyrosine kinases has been implicated in the development and/or progression of a variety of cancers. Studies on ErbB receptors in osteosarcoma have focused on HER-2 and have produced conflicting results with few studies evaluating the expression of the epidermal growth factor receptor (EGFR). In this study, we determined the level of expression of EGFR and the mutational status of the EGFR receptor in a subset of osteosarcoma tumor samples as well as in a series of established bone tumor-derived cell lines. EGFR protein expression was detected in the form of strong membranous staining by immunohistochemistry in 21 (57%) of 37 cases analyzed. Six of 12 (50%) osteosarcoma cell lines revealed moderate to high expression levels of EGFR. Two somatic alterations (E829E and R831C) were identified in the cytoplasmic domain of the EGFR gene in 1 of 10 tumor samples. The significance of these findings for the pathobiology of osteosarcomas will be investigated further.


Asunto(s)
Neoplasias Óseas/metabolismo , ADN de Neoplasias/análisis , Receptores ErbB/metabolismo , Osteosarcoma/metabolismo , Adolescente , Adulto , Western Blotting , Neoplasias Óseas/genética , Neoplasias Óseas/patología , Línea Celular Tumoral , Niño , Análisis Mutacional de ADN , Receptores ErbB/química , Receptores ErbB/genética , Femenino , Humanos , Inmunohistoquímica , Masculino , Osteosarcoma/genética , Osteosarcoma/secundario , Reacción en Cadena de la Polimerasa , Estructura Terciaria de Proteína
9.
Obstet Gynecol ; 110(1): 103-8, 2007 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-17601903

RESUMEN

OBJECTIVE: To report and propose a consensus term for eight cases of a newly recognized, asymptomatic, rapidly growing unilateral labium majus mass without palpable borders in prepubertal girls, appearing to be temporally associated with the physiologic increase of adrenal hormones. METHODS: Histologic examination, special stains, and immunohistochemistry were performed on all cases. In our personal cases, electron microscopy and chromosomal analysis were also performed, together with pelvic magnetic resonance imaging (MRI), inguinal exploration, vaginoscopy with biopsies, and adrenal hormone levels. RESULTS: Of the eight cases, seven were Ashkenazi Jewish girls from the same area in New York City. The unilateral masses were asymptomatic, soft, without palpable borders. The overlying skin had a slightly tan peau d'orange surface. The masses could not be completely excised because they extended into the contiguous pelvic floor. Histologically, the masses were composed of bland hypocellular fibrous tissue extending into the deep subcutaneous tissue. The masses blended into the surrounding tissue and adjacent pelvic floor as shown by MRI preoperatively and postoperatively. Residual tissue did not progress after incomplete resection. CONCLUSION: These fibrous lesions develop in months at the time of physiologic increase in adrenal hormone secretion just before puberty and subsequently appear to stop growing. The surgeon should not attempt a complete removal but simply excise sufficient tissue for a reasonable cosmetic result and to confirm the diagnosis. The lesions reflect fibroblastic hyperplasia, which is possibly hormone-driven. The ethnic and geographic clustering of cases raises consideration of environmental exposures or genetic predisposition.


Asunto(s)
Vulva/patología , Enfermedades de la Vulva/patología , Niño , Preescolar , Femenino , Histocitoquímica , Humanos , Hiperplasia/patología , Judíos/etnología , Ciudad de Nueva York , Pubertad , Enfermedades de la Vulva/etnología
10.
Cancer Res ; 62(9): 2660-8, 2002 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-11980665

RESUMEN

Enhanced expression of tenascin-C (TN-C) at the invasive edges of glioblastoma multiforme in close association with vascular sprouts, suggests a role for TN-C in microvascular cell migration. To test this hypothesis, we studied the migration of endothelial cells in vitro. In an aggregate migration assay, bovine retinal endothelial cells (BRECs) and human umbilical vein endothelial cells spread and migrated similarly on TN-C or fibronectin (FN). In contrast, U251 MG glioma cells migrated less on TN-C than on FN. Morphological features of U251 MG glioma cells on TN-C included poor cell spreading and short processes. In contrast, on FN, U251 MG glioma cells spread and exhibited long radial processes. Using a transmembrane migration assay, we observed that BREC adhesion was similar on TN-C or FN, whereas U251 MG glioma cells adhered better to FN than to TN-C. In addition, BRECs migrated more across the membrane toward regions coated with TN-C than FN, and conversely, U251 MG glioma cells migrated more toward FN than TN-C. Migration of endothelial and glioma cells toward TN-C or FN occurred in a dose-dependent manner and was strongly dependent on cell adhesion. In this assay, ultrastructural study revealed the migrating phenotype of the endothelial cells through the micropores of the membrane and their spread morphology on TN-C. Moreover, in situ hybridization revealed specific expression of TN-C in migrating microvascular cells in a cerebral microvascular ring assay. Finally in a phosphorylation assay, TN-C enhanced focal adhesion kinase phosphorylation of BRECs, but not of U251 MG glioma cells, and FN enhanced focal adhesion kinase phosphorylation of both BRECs and U251 MG cells. The expression of TN-C by migrating endothelial cells and the promotion of endothelial cell adhesion and migration by TN-C suggest a potential role for TN-C in pathological angiogenesis.


Asunto(s)
Movimiento Celular/fisiología , Endotelio Vascular/citología , Proteínas Tirosina Quinasas/metabolismo , Tenascina/fisiología , Animales , Bovinos , Adhesión Celular/fisiología , Endotelio/citología , Endotelio/enzimología , Endotelio/metabolismo , Endotelio Vascular/enzimología , Endotelio Vascular/metabolismo , Quinasa 1 de Adhesión Focal , Proteína-Tirosina Quinasas de Adhesión Focal , Glioma/enzimología , Glioma/metabolismo , Glioma/patología , Humanos , Microscopía Electrónica , Neovascularización Fisiológica/fisiología , Fosforilación , Retina/citología , Retina/enzimología , Retina/metabolismo , Tenascina/biosíntesis
11.
Arch Facial Plast Surg ; 7(5): 326-30, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-16172343

RESUMEN

Lipoblastomas are rare benign tumors of infancy that usually affect children younger than 3 years. Most lipoblastomas (70%) occur on the extremities. Lipoblastomas may mimic other infantile tumors, including hemangiomas, hibernomas, lipomas, and liposarcomas, and correct diagnosis is necessary to ensure appropriate treatment. Lipoblastomas fall under 2 discrete subtypes: well-circumscribed lipoblastomas and diffuse lipoblastomatosis. Both types present with firm, nontender masses of lobulated, well-circumscribed soft tissue. Histologically they can be highly vascularized with plexiform capillaries, often with an individual feeder artery to each lobule. Complete surgical removal is the recommended treatment. Only 2 cases of lipoblastomas of the cheek have been reported in the English-language literature. We present the case of a young child with a cheek lipoblastoma, emphasizing the importance of correct diagnosis and highlighting techniques used to provide suitable treatment.


Asunto(s)
Neoplasias Faciales/patología , Hemangioma/patología , Neoplasias de Tejido Adiposo/patología , Biopsia con Aguja , Preescolar , Diagnóstico Diferencial , Neoplasias Faciales/diagnóstico , Neoplasias Faciales/cirugía , Femenino , Estudios de Seguimiento , Hemangioma/diagnóstico , Hemangioma/cirugía , Humanos , Inmunohistoquímica , Lactante , Recién Nacido , Imagen por Resonancia Magnética/métodos , Masculino , Neoplasias de Tejido Adiposo/diagnóstico , Neoplasias de Tejido Adiposo/cirugía , Medición de Riesgo , Tomografía Computarizada por Rayos X/métodos , Resultado del Tratamiento
12.
J Pediatr Hematol Oncol ; 26(10): 681-685, 2004 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-27811613

RESUMEN

Thymoma is an uncommon tumor of childhood. Stage of the tumor is an independent prognostic factor for survival. Surgery is the treatment of choice for stage I and stage II tumors. Chemotherapy is reserved for patients with refractory or metastatic disease. Thymomas are moderately radiosensitive. However, radiation therapy is not an attractive option for children due to its side-effects on developing organs. The authors describe 2 children with completely encapsulated thymoma who were successfully treated with surgery alone. Both patients remain free of disease 3 years after surgery. One of the patients also has nevus sebaceous. The authors also discuss the possible association between the two disease entities.

13.
Mol Endocrinol ; 25(6): 1018-26, 2011 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-21527502

RESUMEN

Lymphoid enhancer-binding factor (LEF)1 is a major mediator and a target in canonical Wnt/ß-catenin pathway. Interactions between the androgen receptor (AR) and canonical Wnt pathways have been implicated in the development of the genitourinary organs. Here, we investigated the localization and role of LEF1-positive cells during development of the prostate gland in human and in the murine model. We show that during human prostate development, LEF1 is restricted to the basal epithelial layer of the urogenital sinus. During mouse development, Lef1 is also present in the urogenital mesenchyme in addition to the basal epithelial layer of the urogenital sinus. In the course of elongation and branching of the prostatic ducts, Lef1 is localized to the proliferating epithelium at the distal tips of the buds. Notably, during branching morphogenesis, domains of Lef1 and AR are mutually exclusive. We further employed the TOPGAL reporter strain to examine the dynamics of Wnt signaling in the context of prostate regression upon a 7-d treatment with a competitive AR inhibitor, bicalutamide. We found that Wnt/Lef1-positive basal cells are not dependent upon androgen for survival. Furthermore, upon bicalutamide treatment, Wnt/Lef1-positive basal progenitors repopulated the luminal compartment. We conclude that Wnt/Lef1 activity identifies an androgen-independent population of prostate progenitors, which is important for embryonic development and organ maintenance and regeneration in the adult.


Asunto(s)
Epitelio/metabolismo , Factor de Unión 1 al Potenciador Linfoide/metabolismo , Próstata/embriología , Receptores Androgénicos/metabolismo , Animales , Proliferación Celular , Genes Reporteros , Humanos , Queratinas Tipo I/metabolismo , Queratinas Tipo II/metabolismo , Antígeno Ki-67/metabolismo , Masculino , Proteínas de la Membrana/metabolismo , Ratones , Próstata/citología , Próstata/metabolismo , Transducción de Señal , Proteínas Wnt/metabolismo , beta-Galactosidasa/biosíntesis , beta-Galactosidasa/genética
15.
J Pediatr Surg ; 42(12): 2129-31, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18082724

RESUMEN

Concomitant hereditary spherocytosis and sickle cell trait, although extremely rare, could potentially lead to splenic sequestration or infarction. We report here the first case of splenic infarction in a child with hereditary spherocytosis and sickle cell trait while flying on a commercial aircraft. The presence of hypoxia, hemoconcentrated erythrocytes, and sickle hemoglobin created the perfect environment for clinical sequelae.


Asunto(s)
Rasgo Drepanocítico/complicaciones , Esferocitosis Hereditaria/complicaciones , Infarto del Bazo/etiología , Infarto del Bazo/cirugía , Biopsia con Aguja , Niño , Femenino , Estudios de Seguimiento , Humanos , Inmunohistoquímica , Medición de Riesgo , Índice de Severidad de la Enfermedad , Rasgo Drepanocítico/diagnóstico , Esferocitosis Hereditaria/diagnóstico , Esplenectomía/métodos , Infarto del Bazo/patología , Tomografía Computarizada por Rayos X , Resultado del Tratamiento
16.
J Urol ; 177(5): 1918-22, 2007 May.
Artículo en Inglés | MEDLINE | ID: mdl-17437848

RESUMEN

PURPOSE: The role of androgen receptor coactivators in testicular development and cancer formation is unclear. p44/Mep50 was identified as an androgen receptor coactivator that functions in a complex with protein arginine methyltransferase 5. We studied the expression of p44 and protein arginine methyltransferase 5 in developing fetal testis and adult testicular tumors, including seminomas and Leydig cell tumors. MATERIALS AND METHODS: A total of 30 human fetal testes from abortuses at a gestational age of 10 to 40 weeks, 33 human seminomas and 11 human Leydig cell tumors were retrieved from the archives of the departments of pathology. Immunohistochemistry was performed with affinity purified p44 and IgG purified protein arginine methyltransferase 5 polyclonal antibodies. RESULTS: Protein arginine methyltransferase 5 and p44 were expressed predominantly as nuclear proteins in fetal Leydig cells and human adult nonneoplastic testes, including germ cells and Leydig cells, while they were expressed in the cytoplasm of germ cells of the fetal testis. Expression was strongest in the fetal testis during the second trimester. Compared to adult nonneoplastic testes, human seminoma and Leydig tumor cells showed a marked decrease in nuclear expression of p44 and protein arginine methyltransferase 5 with a concomitant marked increase in cytoplasmic expression of these proteins. Furthermore, average testicular size was increased by 29% in p44(+/-) heterzygotic mice. CONCLUSIONS: These results suggest distinct functions of the nuclear and the p44/protein arginine methyltransferase 5 complexes in the developing fetal testis and in the oncogenesis of testicular tumors. Further studies are needed to confirm the functional relevance of these findings.


Asunto(s)
Regulación del Desarrollo de la Expresión Génica , Regulación Neoplásica de la Expresión Génica , Proteína Metiltransferasas/genética , ARN Mensajero/genética , Neoplasias Testiculares/metabolismo , Testículo/metabolismo , Factores de Transcripción/genética , Adulto , Animales , Northern Blotting , Femenino , Humanos , Inmunohistoquímica , Tumor de Células de Leydig/metabolismo , Tumor de Células de Leydig/patología , Masculino , Ratones , Ratones Endogámicos C57BL , Proteína Metiltransferasas/metabolismo , Proteína-Arginina N-Metiltransferasas , Seminoma/metabolismo , Seminoma/patología , Neoplasias Testiculares/patología , Testículo/embriología , Factores de Transcripción/metabolismo
17.
Pediatr Surg Int ; 22(10): 865-8, 2006 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16944181

RESUMEN

Children with acquired immunodeficiency syndrome (AIDS) are at an increased risk for lymphoproliferative and neoplastic disorders. Included among these are smooth muscle neoplasms such as leiomyomas and leiomyosarcomas. There have been at least 15 reported cases of smooth muscle tumors in the approximately 8,000 children with AIDS, however the incidence in immunocompetent children is only two per ten million. The lesions in children with human immunodeficiency virus infection are usually found in the lung, liver, and gastrointestinal tract. Here, we present an unusual case of a 12-year-old African American girl with vertically acquired AIDS who presented to the pediatric emergency department with severe diffuse abdominal pain. She was ultimately found to have an appendiceal leiomyoma on abdominal exploration, the first reported case. Our report suggests that smooth muscle tumors of the appendix be included in the differential diagnosis of abdominal masses in children with AIDS.


Asunto(s)
Síndrome de Inmunodeficiencia Adquirida/complicaciones , Neoplasias del Apéndice/complicaciones , Leiomioma/complicaciones , Neoplasias del Apéndice/diagnóstico , Neoplasias del Apéndice/cirugía , Niño , Diagnóstico Diferencial , Femenino , Estudios de Seguimiento , Humanos , Laparoscopía , Laparotomía , Leiomioma/diagnóstico , Leiomioma/cirugía , Tomografía Computarizada por Rayos X
18.
Pediatr Surg Int ; 22(7): 613-6, 2006 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16633822

RESUMEN

Persistent interstitial pulmonary emphysema (PIPE) is a syndrome characterized by air-leakage in the perivascular tissues of the lung, primarily affecting mechanically ventilated neonates. Reports in the literature of infants developing PIPE with no history of respiratory distress syndrome (RDS) or mechanical ventilation are scarce. Here, we present a case of a 3-month-old former full term male infant with no history of RDS or mechanical ventilation who presented with focal cystic lung disease associated with spontaneous tension pneumothorax. He was ultimately found to have PIPE based on pathologic evaluation of the resected cystic region. We believe that focal PIPE should be included in the differential diagnosis of cystic lung disease in a full term, unventilated infant, even when spontaneous pneumothorax is the presenting entity.


Asunto(s)
Neumotórax/etiología , Enfisema Pulmonar/complicaciones , Humanos , Lactante , Masculino , Nacimiento a Término
19.
Pediatr Dev Pathol ; 8(6): 630-8, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-16328664

RESUMEN

The investigation of sudden death of infants varies, and death rates may depend on local practices of death certification. We studied the extent of the investigation and the final cause of death (COD) in 3 regions: New York, New York, USA (NY); King County, Washington, USA (KC); and Montevideo, Uruguay (MU). We conducted a retrospective review of 543 cases (NY 258, KC 56, MU 229) of previously healthy babies who died suddenly without obvious trauma, at ages 0 to 12 months, over a 3-year period (1998 to 2001). All cases included a complete autopsy and histologic examination. Cases were assessed for completion of special studies (including radiographs, photos, toxicology and metabolic sampling, cultures, and vitreous humor chemistry), measurements, and scene investigation. Specialized pediatric measurements and testing were done less often than routine procedures, and were done less often in cases overall compared with cases certified as sudden infant death syndrome (SIDS). Fifty-five percent of SIDS cases in NYC and 12% of SIDS cases in KC had no scene investigation. Manhattan had a complete workup in 42% of SIDS cases, whereas the remaining sites had fewer that 15% of cases completely worked up. The most common non-natural COD was suffocation at all 3 sites. The overall most common COD were respiratory infection in MU (22%) and SIDS in NY (45%) and KC (86%). We conclude that the sudden death of infants requires special consideration and still lacks consistency. SIDS investigations are not done completely in all cases and rates may depend on regional differences in certifying infant deaths.


Asunto(s)
Causas de Muerte , Muerte Súbita/epidemiología , Muerte Súbita/etiología , Asfixia Neonatal/complicaciones , Asfixia Neonatal/epidemiología , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Infecciones del Sistema Respiratorio/complicaciones , Infecciones del Sistema Respiratorio/epidemiología , Estudios Retrospectivos , Muerte Súbita del Lactante/epidemiología , Muerte Súbita del Lactante/etiología
20.
Pediatr Dev Pathol ; 8(6): 718-24, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-16328671

RESUMEN

Giant cell tumor of soft tissue (GCTST) has gained general acceptance as an uncommon but distinct primary soft tissue tumor since it was first described in 1972. GCTST is predominantly seen in adults and typically shows uniformly dispersed osteoclast-like giant cells admixed with oval to polygonal mononuclear cells. It usually follows a benign clinical course, although the malignant variant has been described in cases in which the mononuclear cells demonstrate obvious dysplastic features. It is still not clear whether the two variants belong to the spectrum of the same tumor. No cytogenetic chromosomal abnormalities have been reported in the literature of GCTST. Interestingly, the osseous counterpart of giant cell tumor, which shares similar histologic features, quite often displays a telomeric association at the cytogenetic level, a finding that has never been reported in GCTST. We report the case of a 12-year-old girl with GCTST of the right leg that metastasized to the lung. Cytogenetic studies from the primary tumor showed the phenomenon of telomeric association involving multiple chromosomes.


Asunto(s)
Tumores de Células Gigantes/genética , Tumores de Células Gigantes/secundario , Neoplasias Pulmonares/genética , Neoplasias Pulmonares/secundario , Neoplasias de los Tejidos Blandos/genética , Neoplasias de los Tejidos Blandos/patología , Niño , Aberraciones Cromosómicas , Femenino , Humanos , Telómero/genética
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