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This release introduced several new features including annotative data links and floating views. It also introduced the line arrow tool. The release was followed by Release 5.1 (revision 9.0) and Release 5.2 (revision 10.0) in June and September 1994, respectively. AutoCAD Release 6 (revision 12.0) was released in October 1996. It introduced three-dimensional (3D) modeling and a geospatial model called AutoCAD Map3D. AutoCAD Release 7 (revision 14.0) was released in October 1999. This release was the first version to be capable of displaying drawings on the World Wide Web. This release also included 2D drafting tools called AutoLISP (i.e., AutoCAD's first 2D drafting tools). AutoCAD Release 8 (revision 15.0) was released in September 2000. It included a new tool that allowed users to interactively change the size of the drawing, as well as tools for measuring and revising the project layout. AutoCAD Release 9 (revision 16.0) was released in August 2001. 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See also Autodesk Vault List of CAD software References External links Autodesk Official site Category:2017 software Category:Computer-aided design software Category:Computer-aided design software for Windows Category:Electronic drawing Category:Information technology companies of the United States Category:Windows graphics-related software Category:Windows-only software Category:Products introduced in 1994 Category:3D graphics software Category:Computer-aided design software for MacOS Category:1994 software Category:2017 mergers and acquisitionsA case of neurofibromatosis 2 presenting with an unusual clinical course. Neurofibromatosis type 2 (NF2) is a rare autosomal dominant disorder characterized by bilateral vestibular schwannomas (neurofibromas), schwannomas of the spinal nerve roots, meningiomas, ependymomas, and pheochromocytomas. This disease is usually diagnosed in early adulthood. We present a case of NF2 presenting with atypical clinical features and unusual clinical course. A 40-year-old woman with a history of NF2 was seen in the neurotologic clinic for evaluation of a sensorineural hearing loss on the left side. Examination revealed a soft, enlarging, fluctuant scalp mass, which had been present for at least 20 years. Further examination revealed a 4.0-cm well-circumscribed, rubbery, grayish-white, soft mass of the left posterior mastoid area that was excised, along with the facial nerve. Histopathology was consistent with a schwannoma, and immunohistochemical staining showed the tumor to be negative for S-100. The postoperative course was uncomplicated, and the patient was neurologically intact at 1-year follow-up. This case of NF2 was characterized by atypical presentation and symptoms, but no associated intracranial lesions, meningioma, or peripheral neuropathy. 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