Lymphaticovenous differentiation in Kaposi's sarcoma. Cellular phenotypes by stage.
Journal: 1988/March - American Journal of Pathology
ISSN: 0002-9440
PUBMED: 3124627
Abstract:
The histogenesis of Kaposi's sarcoma was investigated by immunohistochemical staining of 20 skin specimens that represented four main histologic stages. The early phase of Stage 1 contained lymphatic-like clefts lined by endothelial cells with thin, discontinuous basement membranes shown by anti-laminin, absent Factor VIII-related antigen reactivity (FVIIIRAg), and only rare staining with dilute Ulex europaeus agglutinin I (UEA-I). In the late phase of Stage 1, the clefts developed into anastomosing, blood-filled channels, and the basement membrane became complete. Endothelial marker reactivities were not definitive, but weak staining with UEA-I and variable staining for FVIIIRAg characterized the spindle cells of Stage 2. However, spindle cells in monomorphic nodules were individually enclosed by immunoreactive laminin. The sequence of events, particularly in light of previous angiographic findings of lymphaticovenous union, suggests a disturbance in lymphaticovenous differentiation in Kaposi's sarcoma. Sclerotic closure of channels unable to maintain competent blood flow may select against lymphendothelial traits in the developing spindle cell nodule.
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Am J Pathol 130(2): 411-417

Lymphaticovenous differentiation in Kaposi's sarcoma. Cellular phenotypes by stage.

Abstract

The histogenesis of Kaposi's sarcoma was investigated by immunohistochemical staining of 20 skin specimens that represented four main histologic stages. The early phase of Stage 1 contained lymphatic-like clefts lined by endothelial cells with thin, discontinuous basement membranes shown by anti-laminin, absent Factor VIII-related antigen reactivity (FVIIIRAg), and only rare staining with dilute Ulex europaeus agglutinin I (UEA-I). In the late phase of Stage 1, the clefts developed into anastomosing, blood-filled channels, and the basement membrane became complete. Endothelial marker reactivities were not definitive, but weak staining with UEA-I and variable staining for FVIIIRAg characterized the spindle cells of Stage 2. However, spindle cells in monomorphic nodules were individually enclosed by immunoreactive laminin. The sequence of events, particularly in light of previous angiographic findings of lymphaticovenous union, suggests a disturbance in lymphaticovenous differentiation in Kaposi's sarcoma. Sclerotic closure of channels unable to maintain competent blood flow may select against lymphendothelial traits in the developing spindle cell nodule.

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  • DORFMAN RF. Kaposi's sarcoma. The contribution of enzyme histochemistry to the identification of cell types. Acta Unio Int Contra Cancrum. 1962;18:464–476. [PubMed] [Google Scholar]
  • Palmer PE. Haemangiosarcoma of Kaposi. Acta Radiol Suppl. 1972;316:1–52. [PubMed] [Google Scholar]
  • Dictor M. Kaposi's sarcoma. Origin and significance of lymphaticovenous connections. Virchows Arch A Pathol Anat Histopathol. 1986;409(1):23–35. [PubMed] [Google Scholar]
  • COX FH, HELWIG EB. Kaposi's sarcoma. Cancer. 1959 Mar-Apr;12(2):289–298. [PubMed] [Google Scholar]
  • Costa J, Rabson AS. Generalised Kaposi's sarcoma is not a neoplasm. Lancet. 1983 Jan 1;1(8314-5):58–58. [PubMed] [Google Scholar]
  • Brooks JJ. Kaposi's sarcoma: a reversible hyperplasia. Lancet. 1986 Dec 6;2(8519):1309–1311. [PubMed] [Google Scholar]
  • Rutgers JL, Wieczorek R, Bonetti F, Kaplan KL, Posnett DN, Friedman-Kien AE, Knowles DM., 2nd The expression of endothelial cell surface antigens by AIDS-associated Kaposi's sarcoma. Evidence for a vascular endothelial cell origin. Am J Pathol. 1986 Mar;122(3):493–499.[PMC free article] [PubMed] [Google Scholar]
  • Jones RR, Spaull J, Spry C, Jones EW. Histogenesis of Kaposi's sarcoma in patients with and without acquired immune deficiency syndrome (AIDS). J Clin Pathol. 1986 Jul;39(7):742–749.[PMC free article] [PubMed] [Google Scholar]
  • McNutt NS, Fletcher V, Conant MA. Early lesions of Kaposi's sarcoma in homosexual men. An ultrastructural comparison with other vascular proliferations in skin. Am J Pathol. 1983 Apr;111(1):62–77.[PMC free article] [PubMed] [Google Scholar]
  • Beckstead JH, Wood GS, Fletcher V. Evidence for the origin of Kaposi's sarcoma from lymphatic endothelium. Am J Pathol. 1985 May;119(2):294–300.[PMC free article] [PubMed] [Google Scholar]
  • Burgdorf WH, Mukai K, Rosai J. Immunohistochemical identification of factor VIII-related antigen in endothelial cells of cutaneous lesions of alleged vascular nature. Am J Clin Pathol. 1981 Feb;75(2):167–171. [PubMed] [Google Scholar]
  • Holthöfer H, Virtanen I, Kariniemi AL, Hormia M, Linder E, Miettinen A. Ulex europaeus I lectin as a marker for vascular endothelium in human tissues. Lab Invest. 1982 Jul;47(1):60–66. [PubMed] [Google Scholar]
  • Barsky SH, Baker A, Siegal GP, Togo S, Liotta LA. Use of anti-basement membrane antibodies to distinguish blood vessel capillaries from lymphatic capillaries. Am J Surg Pathol. 1983 Oct;7(7):667–677. [PubMed] [Google Scholar]
  • Ordóez NG, Batsakis JG. Comparison of Ulex europaeus I lectin and factor VIII-related antigen in vascular lesions. Arch Pathol Lab Med. 1984 Feb;108(2):129–132. [PubMed] [Google Scholar]
  • Kramer RH, Fuh GM, Hwang CB, Conant MA, Greenspan JS. Basement membrane and connective tissue proteins in early lesions of Kaposi's sarcoma associated with AIDS. J Invest Dermatol. 1985 Jun;84(6):516–520. [PubMed] [Google Scholar]
  • Bendelac A, Kanitakis J, Chouvet B, Thivolet J. Basement membrane in Kaposi's sarcoma: an immunohistochemical and ultrastructural study. Pathol Res Pract. 1985 Dec;180(6):626–632. [PubMed] [Google Scholar]
  • Guarda LG, Silva EG, Ordóez NG, Smith JL., Jr Factor VIII in Kaposi's sarcoma. Am J Clin Pathol. 1981 Aug;76(2):197–200. [PubMed] [Google Scholar]
  • Modlin RL, Hofman FM, Kempf RA, Taylor CR, Conant MA, Rea TH. Kaposi's sarcoma in homosexual men: an immunohistochemical study. J Am Acad Dermatol. 1983 May;8(5):620–627. [PubMed] [Google Scholar]
  • Nadji M, Morales AR, Ziegles-Weissman J, Penneys NS. Kaposi's sarcoma: immunohistologic evidence for an endothelial origin. Arch Pathol Lab Med. 1981 May;105(5):274–275. [PubMed] [Google Scholar]
  • Millard PR, Heryet AR. An immunohistological study of factor VIII related antigen and Kaposi's sarcoma using polyclonal and monoclonal antibodies. J Pathol. 1985 May;146(1):31–38. [PubMed] [Google Scholar]
  • Braun-Falco O, Schmoeckel C, Hübner G. Zur Histogenese des Sarcoma idiopathicum multiplex haemorrhagicum (Morbus Kaposi): Eine histochemische und elektronenmikroskopische Studie. Virchows Arch A Pathol Anat Histol. 1976 Feb 16;369(3):215–227. [PubMed] [Google Scholar]
  • NIEMI M, MUSTAKALLIO KK. THE FINE STRUCTURE OF THE SPINDLE CELL IN KAPOSI'S SARCOMA. Acta Pathol Microbiol Scand. 1965;63:567–575. [PubMed] [Google Scholar]
  • Lo SC, Liotta LA. Vascular tumors produced by NIH/3T3 cells transfected with human AIDS Kaposi's sarcoma DNA. Am J Pathol. 1985 Jan;118(1):7–13.[PMC free article] [PubMed] [Google Scholar]
  • Delli Bovi P, Donti E, Knowles DM, 2nd, Friedman-Kien A, Luciw PA, Dina D, Dalla-Favera R, Basilico C. Presence of chromosomal abnormalities and lack of AIDS retrovirus DNA sequences in AIDS-associated Kaposi's sarcoma. Cancer Res. 1986 Dec;46(12 Pt 1):6333–6338. [PubMed] [Google Scholar]
  • Miettinen M, Lehto VP, Virtanen I. Postmastectomy angiosarcoma (Stewart-Treves syndrome). Light-microscopic, immunohistological, and ultrastructural characteristics of two cases. Am J Surg Pathol. 1983 Jun;7(4):329–339. [PubMed] [Google Scholar]
  • Chen KT, Gilbert EF. Angiosarcoma complicating generalized lymphangiectasia. Arch Pathol Lab Med. 1979 Feb;103(2):86–88. [PubMed] [Google Scholar]
  • van der Putte SC. The development of the lymphatic system in man. Adv Anat Embryol Cell Biol. 1975;51(1):3–60. [PubMed] [Google Scholar]
  • Templeton AC. Studies in Kaposi's sarcoma. Postmortem findings and disease patterns in women. Cancer. 1972 Sep;30(3):854–867. [PubMed] [Google Scholar]
  • LOTHE F, MURRAY JF. Kaposi's sarcoma: autopsy findings in the African. Acta Unio Int Contra Cancrum. 1962;18:429–452. [PubMed] [Google Scholar]
  • HASHIMOTO K, LEVER WF. KAPOSI'S SARCOMA. HISTOCHEMICAL AND ELECTRON MICROSCOPIC STUDIES. J Invest Dermatol. 1964 Dec;43:539–549. [PubMed] [Google Scholar]
  • Mottaz JH, Zelickson AS. Electron microscope observations of Kaposi's sarcoma. Acta Derm Venereol. 1966;46(2):195–200. [PubMed] [Google Scholar]
  • Harrison AC, Kahn LB. Myogenic cells in Kaposi's sarcoma: an ultrastructural study. J Pathol. 1978 Mar;124(3):157–160. [PubMed] [Google Scholar]
Department of Pathology, University Hospital, Lund, Sweden.
Department of Pathology, University Hospital, Lund, Sweden.
Abstract
The histogenesis of Kaposi's sarcoma was investigated by immunohistochemical staining of 20 skin specimens that represented four main histologic stages. The early phase of Stage 1 contained lymphatic-like clefts lined by endothelial cells with thin, discontinuous basement membranes shown by anti-laminin, absent Factor VIII-related antigen reactivity (FVIIIRAg), and only rare staining with dilute Ulex europaeus agglutinin I (UEA-I). In the late phase of Stage 1, the clefts developed into anastomosing, blood-filled channels, and the basement membrane became complete. Endothelial marker reactivities were not definitive, but weak staining with UEA-I and variable staining for FVIIIRAg characterized the spindle cells of Stage 2. However, spindle cells in monomorphic nodules were individually enclosed by immunoreactive laminin. The sequence of events, particularly in light of previous angiographic findings of lymphaticovenous union, suggests a disturbance in lymphaticovenous differentiation in Kaposi's sarcoma. Sclerotic closure of channels unable to maintain competent blood flow may select against lymphendothelial traits in the developing spindle cell nodule.
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