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1.
World Neurosurg ; 117: 172-177, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29908379

ABSTRACT

BACKGROUND: Neurofibromatosis type 1 (NF1) has been identified as a predisposing factor in the development of pilocytic astrocytoma (PA), a common benign central nervous system tumor. Although this is a common association, simultaneous development of multiple lesions is an infrequent finding, especially in nonoptic and hypothalamic locations. CASE DESCRIPTION: A 41-year-old female patient with NF1 and uncontrolled human immunodeficiency virus (HIV) type 1 infection presented with a first generalized seizure and associated headache and ataxia. Imaging studies revealed 2 large intra-axial PAs, nodular-cystic in the supratentorial compartment and solid in the infratentorial compartment. Both lesions were treated by gross total resection in 2 surgeries performed 1 week apart. Despite their different imaging patterns, the tumors were histologically and genetically identical. CONCLUSIONS: We present a unique case involving 2 histologically and genetically identical PAs occurring simultaneously in supratentorial and infratentorial locations. We suggest that an intrinsic predisposition to tumor development in patients with NF1 might have been enhanced by the HIV-related immunosuppression in this case. Strict oncologic surveillance is essential in patients with a tumor predisposition syndrome combined with immunosuppression.


Subject(s)
Astrocytoma/complications , HIV Infections/complications , Infratentorial Neoplasms/complications , Neoplasms, Multiple Primary/complications , Neurofibromatosis 1/complications , Supratentorial Neoplasms/complications , Adult , Astrocytoma/diagnostic imaging , Astrocytoma/pathology , Astrocytoma/surgery , Brain/diagnostic imaging , Brain/pathology , Brain/surgery , Female , HIV Infections/diagnostic imaging , HIV Infections/pathology , HIV-1 , Humans , Infratentorial Neoplasms/diagnostic imaging , Infratentorial Neoplasms/pathology , Infratentorial Neoplasms/surgery , Neoplasms, Multiple Primary/diagnostic imaging , Neoplasms, Multiple Primary/pathology , Neoplasms, Multiple Primary/surgery , Neurofibromatosis 1/diagnostic imaging , Neurofibromatosis 1/pathology , Supratentorial Neoplasms/diagnostic imaging , Supratentorial Neoplasms/pathology , Supratentorial Neoplasms/surgery
2.
J Neurol Surg Rep ; 78(1): e59-e61, 2017 Jan.
Article in English | MEDLINE | ID: mdl-28326242

ABSTRACT

Background Lobular capillary hemangioma is a rare benign tumor, most frequently located in the head or neck region, the nasal cavity being uncommonly affected. Its etiopathogenesis is not fully established, although traumatic and hormonal factors have been implied. Case Description A 50-year-old female patient underwent an uneventful endoscopic transsphenoidal removal of a pituitary cystic macroadenoma at our institution. Nasal packing was used in postoperative hemostasis. Histopathology was compatible with a gonadotrophin-producing adenoma. One month after the surgery, the patient presented with frequent episodes of epistaxis and a progressively growing nasal mass, which was removed endoscopically. Its pathological examination confirmed a lobular capillary hemangioma. Conclusions The authors present a clinical case combining two possible predisposing factors to the development of a nasal lobular capillary hemangioma: local traumatic injury through surgery and postoperative nasal packing and hormonal influence. This lesion is a rare complication of endoscopic transsphenoidal resections of pituitary adenomas.

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