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      Is Open Access

      Neurofibromatosis Type I Presenting with Incomplete Ileal Volvulus in a Pediatric Patient

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          Abstract

          Patient: Male, 15-year-old

          Final Diagnosis: Incomplete ileal volvulus secondary to a mesenteric plexiform neurofibroma

          Symptoms: Acute • vague abdominal pain • nausea

          Clinical Procedure: —

          Specialty: Radiology

          Objective:

          Rare disease

          Background:

          Neurofibromatosis 1 is a neurocutaneous disorder with multisystemic manifestations. When patients are lacking overt cutaneous manifestations, diagnosis may be delayed and may complicate diagnosis and management of atypical presentations of this disease. It is thus important to strive to obtain relevant and/or complete history to arrive at the appropriate diagnosis. Furthermore, maintaining an index of suspicion in cases of vague abdominal pain may guide the clinician in establishing the correct diagnosis of mesenteric plexiform neurofibroma in the setting of known/presumed neurofibromatosis 1 patients presenting with acute and/or chronic vague abdominal symptoms.

          Case Report:

          This is a case of a teenage boy who presented with acute, vague abdominal pain over a period of 2 weeks. Laboratory tests and physical exam findings in primary and secondary care settings were unremarkable, and thus the patient was discharged home only to continue with abdominal pain, thus seeking additional medical care. After admission to our facility and exhaustive history taking, physical examination, and imaging, a prospective diagnosis of neurofibromatosis with mesenteric neurofibroma was made. Upon surgical exploration, a mesenteric mass with corresponding volvulized, ischemic small bowel was removed. Histopathology confirmed a plexiform neurofibroma. The patient recovered adequately and was discharged home without complications.

          Conclusions:

          This case highlights the importance of exhaustive history taking to obtain an accurate diagnosis as well as the importance of a high index of clinical suspicion for mesenteric neurofibromatosis in patients with presumed or known neurofibromatosis and presenting with vague abdominal symptoms.

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          Most cited references10

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          • Abstract: found
          • Article: not found

          Malignant peripheral nerve sheath tumors.

          Malignant peripheral nerve sheath tumors (MPNST) are uncommon, biologically aggressive soft tissue sarcomas of neural origin that pose tremendous challenges to effective therapy. In 50% of cases, they occur in the context of neurofibromatosis type I, characterized by loss of function mutations to the tumor suppressor neurofibromin; the remainder arise sporadically or following radiation therapy. Prognosis is generally poor, with high rates of relapse following multimodality therapy in early disease, low response rates to cytotoxic chemotherapy in advanced disease, and propensity for rapid disease progression and high mortality. The last few years have seen an explosion in data surrounding the potential molecular drivers and targets for therapy above and beyond neurofibromin loss. These data span multiple nodes at various levels of cellular control, including major signal transduction pathways, angiogenesis, apoptosis, mitosis, and epigenetics. These include classical cancer-driving genetic aberrations such as TP53 and phosphatase and tensin homolog (PTEN) loss of function, and upregulation of mitogen-activated protein kinase (MAPK) and (mechanistic) target of rapamycin (TOR) pathways, as well as less ubiquitous molecular abnormalities involving inhibitors of apoptosis proteins, aurora kinases, and the Wingless/int (Wnt) signaling pathway. We review the current understanding of MPNST biology, current best practices of management, and recent research developments in this disease, with a view to informing future advancements in patient care.
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            • Record: found
            • Abstract: found
            • Article: not found

            Gastrointestinal and retroperitoneal manifestations of type 1 neurofibromatosis.

            Type 1 neurofibromatosis (NF1) is a genetic disease characterized by neoplastic and not neoplastic disorders, involving tissues of neuroectodermal or mesenchymal origin. The mainly involved districts are skin, central nervous system, and eye, and there is a wide range of severity of clinical presentations.
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              • Record: found
              • Abstract: not found
              • Article: not found

              Gastrointestinal involvement in von Recklinghausen's neurofibromatosis.

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                Author and article information

                Journal
                Am J Case Rep
                Am J Case Rep
                amjcaserep
                The American Journal of Case Reports
                International Scientific Literature, Inc.
                1941-5923
                2023
                12 August 2023
                : 24
                : e918041-1-e918041-6
                Affiliations
                [1 ] Department of Diagnostic Radiology, University of Puerto Rico School of Medicine, San Juan, Puerto Rico
                [2 ] University of Puerto Rico School of Medicine, San Juan, Puerto Rico
                [3 ] Department of Pathology, University of Puerto Rico School of Medicine, San Juan, Puerto Rico
                [4 ] Department of Surgery, University of Puerto Rico School of Medicine, San Juan, Puerto Rico
                [5 ] Department of Surgery, University of Puerto Rico Pediatric Hospital, San Juan, Puerto Rico
                Author notes

                Authors’ Contribution:

                [A]

                Study Design

                [B]

                Data Collection

                [C]

                Statistical Analysis

                [D]

                Data Interpretation

                [E]

                Manuscript Preparation

                [F]

                Literature Search

                [G]

                Funds Collection

                Financial support: None declared

                Conflict of interest: None declared

                Corresponding Author: Ricardo R. Rivera Fernández, e-mail: rivera151@ 123456gmail.com
                Article
                918041
                10.12659/AJCR.918041
                10427934
                37571808
                20a070d0-80b2-44e2-a348-fd8ce1b62ada
                © Am J Case Rep, 2023

                This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International ( CC BY-NC-ND 4.0)

                History
                : 11 June 2019
                : 31 October 2019
                : 09 July 2023
                Categories
                Articles

                intestinal obstruction,intestinal volvulus,neurofibroma, plexiform,neurofibromatosis 1

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