View Item 

Show simple item record

A Solitary Variant of Congenital Self-healing Reticulohistiocytosis: Solitary Hasimoto-Prltzker Disease
dc.contributor.authorBerger, Timothy G.en_US
dc.contributor.authorLane, Alfred T.en_US
dc.contributor.authorHeadington, John T.en_US
dc.contributor.authorHartmann, Kipen_US
dc.contributor.authorBerrish, Geneen_US
dc.contributor.authorLevin, Marc W.en_US
dc.contributor.authorDisantagnese, P. Anthonyen_US
dc.contributor.authorSchwartz, Joel L.en_US
dc.contributor.authorLambert, John S.en_US
dc.date.accessioned2010-06-01T20:56:59Z
dc.date.available2010-06-01T20:56:59Z
dc.date.issued1986-06en_US
dc.identifier.citationBerger, Timothy G.; Lane, Alfred T.; Headington, John T.; Hartmann, Kip; Berrish, Gene; Levin, Marc W.; Disantagnese, P. Anthony; Schwartz, Joel L.; Lambert, John S. (1986). "A Solitary Variant of Congenital Self-healing Reticulohistiocytosis: Solitary Hasimoto-Prltzker Disease." Pediatric Dermatology 3(3): 230-236. <http://hdl.handle.net/2027.42/74044>en_US
dc.identifier.issn0736-8046en_US
dc.identifier.issn1525-1470en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/74044
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3523469&dopt=citationen_US
dc.description.abstractFour neonates had solitary, congenital, rapidly growing, spontaneously ulcerating tumors of the face, trunk, and extremities. No extracutaneous involvement was found, and all lesions spontaneously involuted. Mononuclear cells of the cutaneous infiltrate were Langerhans'cells. These findings expand the spectrum of congenital self-healing reticulohistiocytosis.en_US
dc.format.extent4317612 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights1986 Blackwell Scientific Publication, Inc.en_US
dc.titleA Solitary Variant of Congenital Self-healing Reticulohistiocytosis: Solitary Hasimoto-Prltzker Diseaseen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelDentistryen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Pathology and Dermatology, University of Michigan Medical Center, Ann Arboren_US
dc.contributor.affiliationother* Dermatology Service, Department of Medicine, Letterman Army Medical Center, Presidio of San Franciscoen_US
dc.contributor.affiliationotherDepartments of Dermatology, Pediatrics, and Pathology, University of Rochester Medical Center, Rochester, New Yorken_US
dc.contributor.affiliationotherDepartment of Pediatrics, Walter Reed Army Medical Center, Washington, D.C.en_US
dc.contributor.affiliationotherDepartment of Dermatology, University of California Medical Center, San Franciscoen_US
dc.contributor.affiliationotherDermatology Service, Department of Medicine, Tripler Army Medical Center, Honolulu, Hawaiien_US
dc.identifier.pmid3523469en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/74044/1/j.1525-1470.1986.tb00519.x.pdf
dc.identifier.doi10.1111/j.1525-1470.1986.tb00519.xen_US
dc.identifier.sourcePediatric Dermatologyen_US
dc.identifier.citedreferenceKatz S, Kunihiko T, Sachs D. Epidermal Langerhans' cells are derived from cells originating in bone marrow. Nature 1979; 282: 324 – 326.en_US
dc.identifier.citedreferenceWolff K, Stingl G. The Langerhans' cell. J Invest Dermatol 1983; 80: 17 – 20.en_US
dc.identifier.citedreferenceWolff H. Subtle clues to diagnosis of skin disease by electron microscopy. Am J Dermatopathol 1979; 1: 77 – 81.en_US
dc.identifier.citedreferenceHashimoto K, Pritzker M. Electron microscopic study of reticulohistiocytoma. Arch Dermatol 1973; 107: 263 – 270.en_US
dc.identifier.citedreferenceLaugier P, Hunziker N, Laut J, et al. Reticulo-histiocytose d'evolution benigne (type Hashimoto-Pritzker). Ann Dermatol Syph (Paris) 1975; 102: 21 – 35.en_US
dc.identifier.citedreferenceMascaro J, Aliaga A, Mascaro-Galy C. Reticulose congenitale auto-involutive. Ann Dermatol Venereol 1978; 105: 223 – 227.en_US
dc.identifier.citedreferenceRufli T, Fricker H. Kongenitale, selbstheilende Re-tikulohistiozytose. Z Hautkr 1979; 54: 554 – 558.en_US
dc.identifier.citedreferenceBonifazi E, Caputo R, Ceci A, et al. Congenital self-healing histiocytosis. Arch Dermatol 1982; 118: 267 – 272.en_US
dc.identifier.citedreferenceHashimoto K, Griffin D, Kohsbaki M. Self-healing reticulohistiocytosis. Cancer 1982; 49: 331 – 337.en_US
dc.identifier.citedreferenceHashimoto K, Takahashi S, Lee R, et al. Congenital self-healing reticulohistiocytosis. J Am Acad Dermatol 1984; 11: 447 – 454.en_US
dc.identifier.citedreferenceBasset F, Turiaf J. Identification par la microscopie electronique de particules de nature probablement viral dans les lesions granulomateuses d'une histiocy-tose “X” pulmonaire. CR Acad Sci (Paris) 1956; 261: 3701 – 3703.en_US
dc.identifier.citedreferenceBirbeck MS, Breathnach AS, Everall JD. An electron microscope study of basal melanocytes and high-level clear cells (Langerhans' cells) in vitiligo. J Invest Dermatol 1961; 37: 51 – 63.en_US
dc.identifier.citedreferenceNezelof C, Basset F, Rousseau M. Histiocytosis X histogenetic arguments for a Langerhans' cell origin. Biomedicine 1973; 18: 365 – 371.en_US
dc.identifier.citedreferenceLichtenstein L. Histiocytosis X. Arch Pathol 1953; 56: 84 – 102.en_US
dc.identifier.citedreferenceLahey ME. Histiocytosis X – an analysis of prognostic factors. J Pediatr 1975; 87: 184 – 189.en_US
dc.identifier.citedreferenceGreenberger JS, Crocker AC, Vanter G, et al. Results of treatment of 127 patients with systemic histiocytosis (Letterer-Siwe syndrome, SchÜller-Christian syndrome and multifocal eosinophilic granuloma). Medicine 1981; 60: 311 – 338.en_US
dc.identifier.citedreferenceBroadbent V, Daries EG, Heat D, et al. Spontaneous remission of multisystem histiocytosis-X. Lancet 1984; 1: 253 – 254.en_US
dc.identifier.citedreferenceMarsh WL, Lew SW, Heath VC, et al. Congenital self-healing histiocytosis-X. Am J Pediatr Hematol Oncol 1983; 5: 227 – 233.en_US
dc.identifier.citedreferenceOsband ME, Lipton JM, Lavin P, et al. Histiocytosis X. N Engl J Med 1981; 304: 146 – 153.en_US
dc.identifier.citedreferencePritchard J. Histiocytosis X. Natural history and management in childhood. Clin Exp Dermatol 1979; 4: 421 – 433.en_US
dc.identifier.citedreferenceHelwig EB, Hackrey VC. Juvenile xanthogranuloma (nevoxantho-endothelioma). Am J Pathol 1954; 30: 625 – 626.en_US
dc.identifier.citedreferenceRowden G, Conneley EM, Winkelmann RK. Cutaneous histiocytosis-X: the presence of S-100 protein and its use in diagnosis. Arch Dermatol 1983; 119: 553 – 559.en_US
dc.identifier.citedreferenceBarsky BL, Lao I, Bursky S, et al. Benign cephalic histiocytosis. Arch Dermatol 1984; 120: 650 – 655.en_US
dc.identifier.citedreferenceHeadington JT, Rassmussen J, Hashimoto K, et al. Papular infantile xathomatosis (abstr). Arch Dermatol 1984; 120: 1611.en_US
dc.identifier.citedreferenceStateva S, Kiriakow I, Mustakov G. Kongenitale histiocytosis X. Hautarzt 1980; 31: 26 – 29.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
j.1525-1470.1986.tb00519.x.pdf
Size:
4.117MB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe its collections in a way that respects the people and communities who create, use, and are represented in them. We encourage you to Contact Us anonymously if you encounter harmful or problematic language in catalog records or finding aids. More information about our policies and practices is available at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.