We describe the case of a patient diagnosed with neurofibromatosis type1 (NF1) where unusually extensive and multiple osteolytic lesions ofboth jaws consistent with central giant cell granulomas (CGCG) causedmassive bone destruction and left her almost “jawless.” The patient wasa 58-year-old woman who at the age of 15 years was diagnosed withNF1 and at the age of 53 years underwent radiation therapy for nasalobstruction due to CGCG. The most significant intraoral findings werebrown tumors on the maxillary gingiva; bilateral expansion of the hardpalate; and a yellow mass on the floor of the mouth. Head and neckexamination revealed mandibular asymmetry and features consistentwith NF1. Panoramic radiograph and cone beam computed tomographydisc...
Neurofibromatosis (NF) is an AD dysplasi of mesoderm and ectoderm characterized by numerous neurofib...
Giant cell glioblastoma multiforme (GCGBM) is an uncommon subtype within the spectrum of glioblastom...
Neurofibromatosis type 1 (NF1) is a common genetic disease whose dermatological lesions are at the f...
We describe the case of a patient diagnosed with neurofibromatosis type1 (NF1) where unusually exten...
We describe the case of a patient diagnosed with neurofibromatosis type 1 (NF1) where unusually exte...
Background Neurofibromatosis 1 (NF1) is an autosomal dominantly inherited disorder caused by a spec...
Giant cell granuloma (GCG) of the jaw is a rare, well-known feature of neurofibromatosis type 1 (NF1...
Neurofibromatosis type 1 (NF1) is one of the most common inherited syndromes. The literature on cran...
Neurofibrosarcoma is a rare malignant neoplasm of the head and neck region and accounts for 8% to 16...
INTRODUCTION: Neurofibromatosis is a disease that causes various abnormalities such as neurofibroma,...
AbstractWe present a case of a 39-year-old African-American female who presents with a swelling of t...
Neurofibroma(NF) is one of the common well known autosomal dominant inheritable entity with a preval...
19-year-old male patient, known with a diagnosis of neurofibromatosis type 1, presented with a plexi...
Central giant cell granuloma of the jaws. Central giant cell granuloma was classified by the World ...
Neurofibromatosis (NF) is a genetically transmitted autosomal dominant disorder with variable penetr...
Neurofibromatosis (NF) is an AD dysplasi of mesoderm and ectoderm characterized by numerous neurofib...
Giant cell glioblastoma multiforme (GCGBM) is an uncommon subtype within the spectrum of glioblastom...
Neurofibromatosis type 1 (NF1) is a common genetic disease whose dermatological lesions are at the f...
We describe the case of a patient diagnosed with neurofibromatosis type1 (NF1) where unusually exten...
We describe the case of a patient diagnosed with neurofibromatosis type 1 (NF1) where unusually exte...
Background Neurofibromatosis 1 (NF1) is an autosomal dominantly inherited disorder caused by a spec...
Giant cell granuloma (GCG) of the jaw is a rare, well-known feature of neurofibromatosis type 1 (NF1...
Neurofibromatosis type 1 (NF1) is one of the most common inherited syndromes. The literature on cran...
Neurofibrosarcoma is a rare malignant neoplasm of the head and neck region and accounts for 8% to 16...
INTRODUCTION: Neurofibromatosis is a disease that causes various abnormalities such as neurofibroma,...
AbstractWe present a case of a 39-year-old African-American female who presents with a swelling of t...
Neurofibroma(NF) is one of the common well known autosomal dominant inheritable entity with a preval...
19-year-old male patient, known with a diagnosis of neurofibromatosis type 1, presented with a plexi...
Central giant cell granuloma of the jaws. Central giant cell granuloma was classified by the World ...
Neurofibromatosis (NF) is a genetically transmitted autosomal dominant disorder with variable penetr...
Neurofibromatosis (NF) is an AD dysplasi of mesoderm and ectoderm characterized by numerous neurofib...
Giant cell glioblastoma multiforme (GCGBM) is an uncommon subtype within the spectrum of glioblastom...
Neurofibromatosis type 1 (NF1) is a common genetic disease whose dermatological lesions are at the f...