\nThe patient is an elderly woman seen in a clinic because of persistent mid-back pain. She did not return to her primary care physician after this study; little of her history is available. These are the only imaging studies available in her records. \u00a0<\/span><\/p>\n
Radiologic findings<\/span><\/strong> The key to the radiologic diagnosis of this case lies in the non-calcified cutaneous masses of varying sizes. It is easy to assume the masses are within the patient\u2019s thorax but a closer look shows that most are well-defined, have lucent halos around them and, so, are\u00a0 external to the chest wall. They are pathognomonic of von Recklinghausen\u2019s disease (neurofibromatosis type1).\u00a0The patient is osteoporotic and the vertebral compression fractures may be due to this. Radiologic differential diagnosis<\/span><\/strong> Discussion<\/span><\/strong> NF-1 is different from NF-2 although it, too, is inherited by autosomal dominant transmission. NF-2 is less common than NF-1 (1:50,000), is due to defects in chromosome 22 and in it, cutaneous manifestations are rare. The dominant mode of presentation of NF-2 is by central nervous system lesions (approximately 100%). These include schwannomas of cranial and peripheral nerves, meningiomas in the brain and spine (often multiple), nonneoplastic intracranial calcifications (especially choroids plexus), spinal cord ependymomas and secondary changes of the spine.<\/span><\/p>\n \u00a0<\/span> History The patient is an elderly woman seen in a clinic because of persistent mid-back pain. She did not return to her primary care physician after this study; little of her history is available. These are the only imaging studies available in her records. \u00a0 Radiologic findings The radiographs are frontal and lateral views of […]<\/p>\n","protected":false},"author":6,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[48],"tags":[],"class_list":["post-1183","post","type-post","status-publish","format-standard","hentry","category-from-my-teaching-files","pmpro-has-access"],"_links":{"self":[{"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=\/wp\/v2\/posts\/1183","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=\/wp\/v2\/users\/6"}],"replies":[{"embeddable":true,"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1183"}],"version-history":[{"count":20,"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=\/wp\/v2\/posts\/1183\/revisions"}],"predecessor-version":[{"id":2731,"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=\/wp\/v2\/posts\/1183\/revisions\/2731"}],"wp:attachment":[{"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1183"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1183"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.medradclinics.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1183"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
\nThe radiographs are frontal and lateral views of her thoracic spine.\u00a0 They show:\u00a0\u00a0 <\/span>
\n1. Diffuse osteopenia. <\/span>
\n2. Levoscoliosis of the mid and lower thoracic spine. <\/span>
\n3. Compression fractures of the eighth and ninth thoracic vertebrae. <\/span>
\n4. Numerous round well-defined soft-tissue masses attached to the chest wall. <\/span><\/p>\n
\n<\/span><\/p>\n![\"Neurofibromatosis\"](\"\/wp-content\/uploads\/2013\/06\/Neurofibromatosis-300x208.jpg\")
<\/p>\n
\nVertebral compression fractures are common in the elderly, especially in the setting of osteoporosis. They may also occur in conditions that weaken the vertebrae such as metastatic disease, infection, Scheuermann\u2019s disease (multiple, contiguous intraosseous herniation of nucleus pulposus at the center of weakened endplates (multiple Schmorl\u2019snodes)), sickle-cell anemia and histiocytosis X. Again, the cutaneous masses make the diagnosis easy. \u00a0 Scoliosis and kyphoscoliosis of the spine may be congenital or acquired. When congenital they are due to failure of segmentation or formation of vertebral bodies; they may be mixed, showing features of both. \u00a0 There are many acquired causes of scoliosis and kyphoscoliosis (see below) and painful conditions and von Recklinghausen disease are two such entities.\u00a0 The upper and lower vertebrae in the patient show subtle signs of formation failure suggesting that in her the scoliosis is congenital (a component of the von Recklinghausen conundrum). Clearly, pain from the compression fractures may contribute to the abnormal spinal curvature. Thus, in the patient, congenital and acquired scoliosis may be at play. \u00a0<\/span><\/p>\n
\nFor multiple cutaneous masses<\/strong>: <\/span>
\nThe cutaneous masses in this patient are pathognomonic for neurofibromatosis <\/span>
\nFor scoliosis:<\/span><\/strong>
\n1.<\/span> Mesodermal and neuroectodermal diseases including neurofibromatosis, Marfan’s syndrome,\u00a0\u00a0 homocystinuria.<\/span>
\n 2. Neuromuscular diseases such as myelomeningocele, spinal muscular atrophy, Friedrich’s ataxia, poliomyelitis, cerebral palsy, and muscular dystrophy.
\n3. <\/span>Painful scoliosis as in osteoid osteoma, osteoblastoma, intraspinal tumor, and infection. <\/span>
\n4.<\/span> Congenital scoliosis due to failure of formation, failure of segmentation, or mixed defects. <\/span>
\nFor multiple collapsed vertebrae: <\/span><\/strong>
\n1.<\/span> Osteoporosis <\/span>
\n2. Neoplastic disease <\/span>
\n3. Scheuermann disease<\/span>
\n4.<\/span> Infection<\/span>
\n5. Histiocytosis X <\/span>
\n6.<\/span> Sickle-cell anemia<\/span><\/p>\n
\nNeurofibromatosis type 1 (NF1) is the most common of the phakomatoses, a heterogeneous group of histiogenetic disorders characterized by the presence of central nervous system and, for the most part, cutaneous manifestations. Many also have prominent visceral and connective tissue abnormalities.
\n<\/span><\/p>\n\n
\n Neurofibromatosis<\/span>
\n\u00a0\u00a0\u00a0 Neurofibromatosis type 1<\/span>
\n\u00a0\u00a0\u00a0 Neurofibromatosis type 2<\/span>
\n\u00a0\u00a0\u00a0 Segmental neurofibromatosis.<\/span>
\nVon Hippel-Lindau syndrome<\/span>
\nSturge-Webber syndrome<\/span>
\nTuberous sclerosis<\/span>
\nOthers<\/span>
\n\u00a0\u00a0\u00a0 Ataxia-Telangiectasia<\/span>
\n\u00a0\u00a0\u00a0 Rendu-Osler-Weber<\/span>
\n\u00a0\u00a0\u00a0 Klippel-Trenaunay-Weber<\/span>
\n\u00a0\u00a0\u00a0 Neurocutaneous melanosis<\/span>
\n\u00a0\u00a0\u00a0 Wyburn-Masosn Basal Cell Nevus<\/span>
\n\u00a0\u00a0\u00a0 Cowden Disease.<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
\nNF-1 occurs in one of 2000 to 3000 births. It is inherited by autosomal dominant transmission but has a high spontaneous mutation rate (50%) so that it may occur in offsprings of unaffected parents. The penetrance of the disease is high but its expressivity variable. The problem in the disease lies in the long arm of chromosome 17; there is neuroectodermal and mesodermal tissue dysplasia with potential for diffuse systemic involvement. Males and females are affected equally.<\/span>
\n\u00a0<\/span>
\nThe clinical diagnosis of the disease hinges upon the demonstration of the characteristic cutaneous manifestations or two of the set of criteria shown below. The case in question has numerous cutaneous masses that are consistent with disease although we do not have a full account of the patient\u2019s history.<\/span>
\n\u00a0<\/span>
\n\u00a0The NIH Consensus Development Panel developed a set of diagnostic criteria for NF-1 that includes the following:<\/span>
\n\u00a01.\u00a0<\/span>6 or more 5mm or larger caf\u00e9-au-lait spots. <\/span>
\n\u00a02.\u00a01 plexiform neurofibroma or two or more neurofibromas of any type. <\/span>
\n\u00a03.\u00a0\u00a02 or more pigmented iris hamartomas (so-called Lisch nodules).<\/span>
\n\u00a04.\u00a0\u00a0Axillary or inguinal region freckling.<\/span>
\n\u00a05.\u00a0\u00a0Optic nerve glioma<\/span>
\n\u00a06.\u00a0\u00a0First-degree relative with NF-1<\/span>
\n\u00a07.\u00a0\u00a0Presence of a characteristic bone lesion (e.g. dysplasia of the greater wing of the sphenoid, pseudoarthrosis).<\/span>
\n\u00a0<\/span>
\nThe disease may affect many organs including the brain, spinal cord, peripheral nerves, bones, the dura, the eye and the blood vessels (see below).<\/span><\/p>\n\n
\n Non-CNS lesions<\/span>
\n\u00a0\u00a0\u00a0 Visceral and endocrine tumors:<\/span>
\n\u00a0\u00a0\u00a0 MEA IIb<\/span>
\n\u00a0\u00a0\u00a0 Musculoskeletal lesions:<\/span>
\n\u00a0\u00a0\u00a0 Ribbon ribs<\/span>
\n\u00a0\u00a0\u00a0 Pseudoarthroses<\/span>
\n\u00a0\u00a0\u00a0 Tibial bowing<\/span>
\n\u00a0\u00a0\u00a0 Focal overgrowth of digit, ray or limb<\/span>
\nCNS lesions<\/span>
\n\u00a0\u00a0\u00a0 Optic glioma<\/span>
\n\u00a0\u00a0\u00a0 Nonoptic glioma<\/span>
\n\u00a0\u00a0\u00a0 Basal ganglionic and white matter hamartomas<\/span>
\n\u00a0\u00a0\u00a0 Spinal cord, roots\/ peripheral nerves:<\/span>
\n\u00a0\u00a0\u00a0 Hamartomas<\/span>
\n\u00a0\u00a0\u00a0 Cord astrocytoma<\/span>
\n\u00a0\u00a0\u00a0 Neurofibromas<\/span>
\n\u00a0\u00a0\u00a0 Osseous and dural lesions:<\/span>
\n\u00a0\u00a0\u00a0 Hypoplasia of the greater wing of the sphenoid bone<\/span>
\n\u00a0\u00a0\u00a0 Sutural defects<\/span>
\n\u00a0\u00a0\u00a0 Kyphoscoliosis<\/span>
\n\u00a0\u00a0\u00a0 Meningoceles<\/span>
\n\u00a0\u00a0\u00a0 Ocular\/orbital manifestations:<\/span>
\n\u00a0\u00a0\u00a0 Optic nerve glioma<\/span>
\n\u00a0\u00a0\u00a0 Lisch nodules<\/span>
\n\u00a0\u00a0\u00a0 Buphthalmos<\/span>
\n\u00a0\u00a0\u00a0 Retinal phakomas<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
\nReferences<\/span><\/strong>
\n1. Smirniotopoulos JG, Murphy FM: The phakomatoses, AJNR 13: 725-746, 1992.<\/span>
\n2. Huson SM, Harper PS, Compston DA: von Recklinghausen neurofibromatosis: a clinical and population study in southeast Wales, Brain 111:1355-1381, 1988.<\/span>
\n3. National Institute of Health\u00a0 Consensus Development Conference: Neurofibromatosis Conference Statement, Arch Neurol 45: 579-588, 1988<\/span>
\n4. Diagnostic Neuroradiology, Anne G. Osborn<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"