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Neutrophil Extracellular Traps are Involved in the Innate Immune Response to Infection with Leptospira
- E. Scharrig, A. Carestia, +6 authors R. Gómez
- Biology, Medicine
- PLoS neglected tropical diseases
- 1 July 2015
The data suggest that LIC triggers NETs, and that the intravascular formation of these DNA traps appears to be critical not only to prevent early leptospiral dissemination but also to preclude further bacterial burden. Expand
Extracutaneous infantile haemangioma is also Glut1 positive
All infantiles haemangiomas were immunohistochemically positive for Glut1: expression of this molecule was not limited to infantile haem Mangiomas of the skin, and these tumours comprise proliferations of both endothelial and pericytic cells. Expand
Multilocular cystic renal cell carcinoma : a report of 45 cases of a kidney tumor of low malignant potential.
- S. Suzigan, A. Lopez‐Beltran, +11 authors Maria J. Requena-Tapias
- American journal of clinical pathology
- 1 February 2006
All 45 patients were alive with no evidence of disease at mean follow-up of 66.1 months, confirming an extremely good prognosis after surgery and a 5-year disease-specific survival rate of 100%. Expand
Metastatic Metanephric Adenoma with Foci of Papillary Carcinoma in a Child
- R. Drut, R. Drut, C. Ortolani
- Medicine, Biology
- International journal of surgical pathology
- 1 July 2001
Histology of the primitive tumor resembled the epithelial component of the so-called metanephric adenofibroma while the metastatic lymph node exhibited histologic and FISH genomic features of metamorphic adenoma. Expand
Mesenchymal hamartoma of the chest wall: a cooperative study with review of the literature.
The clinicopathologic features of three examples of mesenchymal hamartoma of the chest wall are described and it is suggested that the lesion should be distinguished from aneurysmal bone cyst, chondroma, and other mesenchyme neoplasms. Expand
Hemorrhagic colitis in postdiarrheal hemolytic uremic syndrome: retrospective analysis of 54 children
Most patients with HC had prominent abdominal findings, and almost 2/3 patients required surgery, and most had long-lasting anuria and severe neurologic involvement. Expand
Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA gene.
- Yu Sun, R. Almomani, +12 authors M. Breuning
- Biology, Medicine
- American journal of human genetics
- 9 July 2010
The data show that TOD is caused by this single recurrent mutation in the FLNA gene, and it is shown that, because of nonrandom X chromosome inactivation, the mutant allele was not expressed in patient fibroblasts. Expand
Malignant ectomesenchymoma in childhood.
- S. Mouton, H. Rosenberg, M. Cohen, R. Drut, M. Emms, R. Kaschula
- Biology, Medicine
- Pediatric pathology & laboratory medicine…
- 1 July 1996
It is implied that because the biological behavior and morphology closely resemble those of rhabdomyosarcoma and because the neurogenic component is often inconspicuous, many malignant ectomesenchymomas may be misdiagnosed as rhabdomsarcomas. Expand
Pseudosarcomatous myofibroblastic proliferations in the urinary bladder of children
Ten examples of a pseudosarcomatous myofibroblastic proliferation occurring in the urinary bladder children (aged 2 to 16 years) are reported and none of the eight patients for whom follow‐up information is available has had local recurrence or metastasis develop 18 months to 6 years after surgical excision. Expand
Presence of human papillomavirus in extrahepatic biliary atresia.
- R. Drut, R. Drut, M. A. Gómez, E. Cueto Rúa, M. Lojo
- Journal of pediatric gastroenterology and…
- 1 November 1998
The high prevalence of human papillomavirus DNA in liver tissue in cases of extrahepatic biliary atresia suggests a strong correlation between this disorder and idiopathic neonatal giant cell hepatitis. Expand