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Journal of Pediatric Surgery
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    • Online Exclusives
    • Sola, Juan ERemove Sola, Juan E filter
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    • Rapid Communication6

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    Author

    • Casillas, Javier3
    • Neville, Holly L3
    • Rodriguez, Maria M3
    • Alvarez, Ofelia A2
    • Thompson, William R2
    • Birusingh, Rhea1
    • Cheung, Michael C1
    • Ciancio, Gaetano1
    • Cova, Deborah1
    • Fields, Jonathan M1
    • Gutierrez, Juan C1
    • Hogan, Anthony R1
    • Huaco, Jorge1
    • Nuwayhid, Zaher1
    • Prescott, Angela1
    • Qualman, Stephen1
    • Rojas, Claudia P1
    • Ryan, Mark L1
    • Vigoda, Michael1
    • Zhuge, Ying1

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    • Journal of Pediatric Surgery6

    Keyword

    • Pediatric2
    • Adolescent1
    • Air embolism1
    • Glomus tumor1
    • Intussusception1
    • Kidney1
    • Laparoscopy1
    • Multiple endocrine neoplasia1
    • Nephron-sparing surgery1
    • Obstruction1
    • Pacifier1
    • Pancreatic islet cell carcinoma1
    • Pediatric malignancy1
    • Pediatrics1
    • Penis amputation1
    • Pheochromocytoma1
    • Pneumatic reduction1
    • Portal venous gas1
    • Renal tumor1
    • Rhabdomyosarcoma1
    • Safety1
    • Thrombotic cutaneous gangrene1
    • Ulcerative colitis1
    • Wilms' tumor1

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    • Rapid Communication

      Portal venous gas and cardiopulmonary arrest during pneumatic reduction of an ileocolic intussusception

      Journal of Pediatric Surgery
      Vol. 46Issue 4e5–e8Published in issue: April, 2011
      • Mark L. Ryan
      • Jonathan M. Fields
      • Juan E. Sola
      • Holly L. Neville
      Cited in Scopus: 4
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        We present the case of an 8-month-old infant with a small bowel obstruction secondary to an ileocolic intussusception without a pathologic lead point. During pneumatic reduction, the patient went into cardiopulmonary arrest, at which point portal venous gas (PVG) was visualized on radiography. Here we present—to our knowledge—the first reported case of PVG secondary to pneumatic reduction of an intussusception along with a review of the literature regarding known complications of pneumatic reduction and the etiologies of PVG.
        Portal venous gas and cardiopulmonary arrest during pneumatic reduction of an ileocolic intussusception
      • Rapid Communication

        Renal glomus tumor in an adolescent: a conservative approach

        Journal of Pediatric Surgery
        Vol. 45Issue 6e23–e26Published in issue: June, 2010
        • Zaher Nuwayhid
        • Maria M. Rodriguez
        • Angela Prescott
        • Gaetano Ciancio
        • Claudia P. Rojas
        • Javier Casillas
        • and others
        Cited in Scopus: 5
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          The most common renal neoplasms in the second decade of life are renal cell carcinomas and Wilms' tumors. Glomus tumors arising in the kidney are rare. We report an adolescent with a benign renal glomus tumor excised by wedge resection. Nephron-sparing surgery is the therapy of choice for children with benign renal tumors. Glomus tumor should be considered in the differential diagnosis of a renal mass in a young patient.
          Renal glomus tumor in an adolescent: a conservative approach
        • Rapid Communication

          Thrombotic cutaneous gangrene with autoamputation of the penis: a rare extracolonic manifestation of ulcerative colitis in a child

          Journal of Pediatric Surgery
          Vol. 44Issue 3e1–e4Published in issue: March, 2009
          • Ying Zhuge
          • Anthony R. Hogan
          • Michael C. Cheung
          • Holly L. Neville
          • William R. Thompson
          • Rhea Birusingh
          • and others
          Cited in Scopus: 5
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            We present a pediatric patient with ulcerative colitis who developed thrombotic cutaneous gangrene involving skin of the lower chest, abdomen, back, bilateral buttocks, bilateral thighs, perineum, and genitalia, ultimately resulting in autoamputation of the glans penis. After an extensive review of the literature, we describe the diagnosis and management of this devastating condition.
            Thrombotic cutaneous gangrene with autoamputation of the penis: a rare extracolonic manifestation of ulcerative colitis in a child
          • Rapid Communication

            Wilms' tumor, pancreatic islet cell carcinoma, and pheochromocytoma in a child

            Journal of Pediatric Surgery
            Vol. 43Issue 3e25–e29Published in issue: March, 2008
            • Juan E. Sola
            • Juan C. Gutierrez
            • William R. Thompson
            • Ofelia A. Alvarez
            • Javier Casillas
            • Maria M. Rodriguez
            Cited in Scopus: 1
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              We present the first case of Wilms' tumor, pancreatic islet cell carcinoma, and pheochromocytoma affecting the same individual. This case underscores the importance of repeat biopsies in patients with multiple neoplasms to confirm the diagnosis and guide management.
              Wilms' tumor, pancreatic islet cell carcinoma, and pheochromocytoma in a child
            • Rapid Communication

              Pacifier-induced bowel obstruction—not so soothing

              Journal of Pediatric Surgery
              Vol. 43Issue 2e13–e15Published in issue: February, 2008
              • Holly L. Neville
              • Jorge Huaco
              • Michael Vigoda
              • Juan E. Sola
              Cited in Scopus: 4
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                Pacifiers are nearly ubiquitous among children in the United States, and although safety regulations exist, the responsibility to choose and maintain a safe pacifier generally falls on the parents, many of whom are unaware of potential hazards. We report a case of a complete bowel obstruction because of an ingested pacifier nipple and recommend increased awareness among practitioners as well as education of parents.
                Pacifier-induced bowel obstruction—not so soothing
              • Rapid Communication

                Primary renal botryoid rhabdomyosarcoma: diagnosis and outcome

                Journal of Pediatric Surgery
                Vol. 42Issue 12e17–e20Published in issue: December, 2007
                • Juan E. Sola
                • Deborah Cova
                • Javier Casillas
                • Ofelia A. Alvarez
                • Stephen Qualman
                • Maria M. Rodriguez
                Cited in Scopus: 11
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                  Primary renal rhabdomyosarcoma is a rare entity. We report on a pediatric patient who, despite having multiple metastases to the lung on presentation, is free of disease 28 months after radical nephrectomy combined with chemotherapy and radiation therapy.
                  Primary renal botryoid rhabdomyosarcoma: diagnosis and outcome
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