1.Piebaldism with Neurofibromatosis Type I: A Familial Case.
Sang Yeon PARK ; Hyun Jung KIM ; Sung Ku AHN
Annals of Dermatology 2014;26(2):264-266
No abstract available.
Neurofibromatosis 1*
;
Piebaldism*
2.Multiple Myxoid Neurofibromas on the Trunk of a Man of Neurofibromatosis Type 1.
Hye Min LEE ; Joong Sun LEE ; Dae Won KOO
Korean Journal of Dermatology 2012;50(9):839-841
No abstract available.
Neurofibroma
;
Neurofibromatoses
;
Neurofibromatosis 1
3.A case of atypical neurofibromatosis type 1.
Eun Joo CHOI ; Young Hyuk LEE ; Min Hee KIM ; Kyo Sun KIM
Journal of the Korean Pediatric Society 1991;34(7):1034-1039
No abstract available.
Neurofibromatoses*
;
Neurofibromatosis 1*
4.Malignant schwannoma associated with von Recklinghausen's disease: Report of 1 case.
Jung Dae OH ; Young Shik LEE ; Seog Hyoo LEE ; Joong Geun CHOI
The Journal of the Korean Orthopaedic Association 1993;28(2):819-823
No abstract available.
Neurilemmoma*
;
Neurofibromatosis 1*
5.A case of neurofibromatosis type 1.
Ji Soon LEE ; Tae Seon YOO ; Seok Kyung HONG ; Hoon Shik YANG
Korean Journal of Otolaryngology - Head and Neck Surgery 1992;35(1):133-138
No abstract available.
Neurofibromatoses*
;
Neurofibromatosis 1*
7.Intracranial colloid cyst in a young female with neurofibromatosis type 1: A case report.
Karlo Angelo F. Camagay ; John Harold Hiyadan
Philippine Journal of Neurology 2020;23(2):15-21
INTRODUCTION:
Intracranial colloid cysts are rare benign tumors located in the region around the foramen of Monro or
around the third ventricle with an annual incidence of 3 of 1,000,000. The common clinical picture is a
progressive headache due to the rapid enlargement of the cyst, resulting in hydrocephalus as it obstructs the cerebrospinal flow; brain herniation may ensue, leading to death.
OBJECTIVES:
The objectives of this report are to (1) present a case of intracranial colloid cyst in a young female with
neurofibromatosis type 1, (2) emphasize the importance of early diagnosis by clinical signs and symptoms and (3) highlight the importance of neuroimaging in arriving at a neurologic diagnosis.
CASE REPORT:
A nineteen-year-old female was seen due to a three-month history of progressive headache, with
associated signs of increased intracranial pressure and with a medical history of neurofibromatosis type 1, inherited from her mother. Neurologic findings revealed papilledema and 6th cranial nerve palsy. By radiographic imaging with clinical correlation, patient was diagnosed with a colloid cyst obstructing the foramen of Monro. Surgical intervention was done and patient improved without complications.
DISCUSSION
Neurofibromatosis is a hereditary neurocutaneous syndrome in which the skin, nervous system, bones,
endocrine glands and sometimes other organs are the sites of a variety of congenital abnormalities, often
taking the form of benign tumors. Intracranial colloid cyst was seen in this case report. Colloid cysts have
an incidence of 0.5 – 1% of all primary brain tumors and are the most common masses in the third
ventricle and in the Foramen of Monro. They cause obstruction of CSF flow, resulting in hydrocephalus.
No published case of neurofibromatosis type 1 patients with a symptomatic intracranial colloid cyst has
been reported yet. Surgical resection is the treatment of choice for colloid cyst.
Neurofibromatosis 1
;
Hydrocephalus
9.Multiple Intracranial Meningiomas: Case Report.
Chang Seong CHO ; Jung Ha PARK ; Sun Wok CHOI ; Kwan Young SONG ; Choong Hyun KIM ; Young Il HA
Journal of Korean Neurosurgical Society 1996;25(9):1923-1928
Meningioma is the third most common intracranial tumor and different from meningiomatosis and multiple meningiomas. Multiple meningiomas without the stigma of Von Recklinghausen's disease are rare. The incidence of multiple meningiomas has been reported in 1-8.9% of all intracranial meningiomas. Although the pathogenic factors related to the multiple meningiomas are unknown, various theories have been studied and reported. The authors report two cases with multiple meningiomas without evidence of the Von Recklinghausen's diseases treated successfully by staged operation. The clinical, radiological and histopathological features of these lesions are discussed.
Incidence
;
Meningioma*
;
Neurofibromatoses
;
Neurofibromatosis 1
10.A Case of Multiple Mendingiomas.
Jang Ho BAE ; Seung Chan BEAK ; Jowa Hyuk IHM ; Oh Lyong KIM ; Yong Chul CHI ; Byung Yearn CHOI ; Soo Ho CHO
Yeungnam University Journal of Medicine 1988;5(2):195-200
The incidence of multiple meningiomas found prior to the introduction of CT was 1~2%, the incidence since the introduction of CT was 8.9%. The authors report a case of multiple meningiomas without evidence of von Recklinghausen's disease. The possible presence of more than 1 tumor in a patient with an intracranial meningiomas must always be kept in mind. The pathogenetic factors related to true multiple meningiomas in unknown. We report a patient with multiple meningiomas which was confirmed by operation.
Humans
;
Incidence
;
Meningioma
;
Neurofibromatosis 1