Abstract
Table 1 summarizes a series of disparate disorders that have been erroneously considered as vascular neoplasms and are described in this chapter.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Kimura T, Yoshimura S, Ishikama E. On the unusual granulation combined with hyperplastic changes of lymphatic tissues. Trans Soc Pathol Jpn 1948;37:178–80.
Kung ITM, Gibson JB, Bannatyne PM. Kimura’s disease: a clinicopathological study of 21 cases and its distinction from angiolymphoid hyperplasia with eosinophilia. Pathology 1984;16:39–44.
Googe PB, Harris NL, Mihn, MC Jr. Kimura’ s disease and angiolymphoid hyperplasia with eosinophilia: two distinct histopathological entities. J Cutan Pathol 1987;14:263–71.
Urabe A, Tsuneyoshi M, Enjoji M. Epithelioid hemangioma versus Kimura’ s disease: a comparative clinicopathologic study. Am J Surg Pathol 1987;11:758–66.
Kuo T-T, Shih L-Y, Chan H-L. Kimura’s disease. Involvement of regional lymph nodes and distinction from angiolymphoid hyperplasia with eosinophilia. Am J Surg Pathol 1988;12:843–54.
Chan JKC, Ng CS, Yuen NWF, Kung ITM, Gwi G. Epithelioid hemangioma (angiolymphoid hyperplasia with eosinophilia) and Kimura’s disease in Chinese. Histopathology 1989;15:557–74.
Hui PK, Chan JK, Ng CS, et al. Lymphadenopathy of Kimura’ s disease. Am J Surg Pathol 1989; 13:177–86.
Chun SI, Ji HG. Kimura’ s disease and angiolymphoid hyperplasia with eosinophilia: clinical and histopathologic differences. J Am Acad Dermatol 1992;27:954–8.
Wells GC, Whimster IW. Subcutaneous angiolymphoid hyperplasia with eosinophilia. Br J Dermatol 1969;81:1–15.
Reed RJ, Terazakis N. Subcutaneous angioblastic lymphoid hyperplasia with eosinophilia (Kimura’ s disease). Cancer 1972;29:489–97.
Kim BM, Sithian N, Cucolo GF. Subcutaneous angiolymphoid hyperplasia (Kimura’s disease). Report of a case. Arch Surg 1975;110:1246–8.
Buchner A, Silverman Jr S, Wara WM, Hansnen LS. Angiolymphoid hyperplasia with eosinophilia (Kimura’ s disease). Oral Surg 1980;49:309–13.
Thompson JW, Colman M, Williamson C, Ward PH. Angiolymphoid hyperplasia with eosinophilia of the external ear canal. Treatment with laser excision. Arch Otolaryngol 1981;107:316–9.
Olsen TG, Helwig EB. Angiolymphoid hyperplasia with eosinophilia: a clinicopathologic study of 116 patients. J Am Acad Dermatol 1985;12:781–96.
Eisenberg, E, Lowlicht R. Angiolymphoid hyperplasia with eosinophils: a clinicopathologic conference. J Oral Pathol 1985;14:216–23.
Rosai J, Gold J, Landy R. The histiocytoid hemangiomas. A unifying entity embracing several previously described entities of the skin, soft tissue, large vessels, bone, and heart. Hum Pathol 1979; 10:707–30.
Rosai J. Angiolymphoid hyperplasia with eosinophilia of the skin. Its nosological position in the spectrum of the histiocytoid hemangioma. Am J Dermatopathol 1982;4:175–84.
Helander SD, Peters MS, Kuo T-T, Su WPD. Kimura’ s disease and angiolymphoid hyperplasia with eosinophilia: new observations from immunohistochemical studies of lymphocyte markers, endothelial antigens, and granulocyte proteins. J Cutan Pathol 1995;22:319–26.
Katagiri K, Itami S, Hatano Y, Yamaguchi T, Takayasu S. In vivo expression of IL-4, IL-5, IL-13 and IFN-gamma mRNAs in peripheral blood mononuclear cells and effect of cyclosporin A in a patient with Kimura’ s disease. Br J Dermatol 1997;137:972–7.
Sugaya M, Suzuki T, Asahina A, Nakamura K, Ohtsuki M, Tamaki K. Kimura’ s disease associated with ulcerative colitis: detection of IL-5 mRNA expression of peripheral blood mononuclear cells and colon lesion. Acta Derm Venereol 1998;78:375–7.
Hongcharu W, Baldassano M, Taylor CR. Kimura’ s disease with oral ulcers: response to pentoxifylline. J Am Acad Dermatol 2000;43:905–7.
Weiss SW, Enzinger FM. Epithelioid hemangioendothelioma. A vascular tumor often mistaken for a carcinoma. Cancer 1982;50:970–81.
Weiss SW, Ishak KG, Dial DH, Sweet DE, Enzinger FM. Epithelioid hemangioendothelioma and related lesions. Semin Diagn Pathol 1986;3:259–87.
Wong KT, Shamsol S. Quantitative study of mast cells in Kimura’s disease. J Cutan Pathol 1999;26:13–6.
Aoki M, Kawana S. The ultrastructural patterns of mast cell degranulation in Kimura’s disease. Dermatology 1999;199:35–9.
Jang KA, Ahn SJ, Choi JH, et al. Polymerase chain reaction (PCR) for human herpesvirus 8 and heteroduplex PCR for clonality assessment in angiolymphoid hyperplasia with eosinophilia and Kimura’ s disease. J Cutan Pathol 2001;28:363–7.
Nagore E, Llorca J, Sanchez-Motilla JM, Ledesma E, Fortea JM, Aliaga A. Detection of Epstein-Barr virus DNA in a patient with Kimura’ s disease. Int J Dermatol 2000;39:618–20.
Kaneko K, Aoki M, Hattori S, Sato M, Kawana S. Successful treatment of Kimura’ s disease with cyclosporine. J Am Acad Dermatol 1999;41:893–4.
Wick MR, Rocamora A. Reactive and malignant “angioendotheliomatosis”: a discriminant clinicopathologic study. J Cutan Pathol 1988;15:260–71.
Ansell J, Bhawan J, Cohen S, et al. Histiocytic lymphoma and malignant angioendotheliomatosis. One disease or two? Cancer 1982;50:1506–12.
Scott PWB, Silvers DN, Helwig EB. Proliferating angioendotheliomatosis. Arch Pathol 1975;99:323–6.
Braverman I, Lerner AB. Diffuse malignant proliferation of vascular endothelium. A possible new clinical and pathologic entity. Arch Dermatol 1961;84:72–80.
Yamamura Y, Akamizu H, Hirata T, Kito S, Hamada T. Malignant lymphoma presenting with neoplastic angioendotheliosis of the central nervous system. Clin Neuropathol 1983:2:62–8.
Wick MR, Scheithaver BW, Okazaki H, et al. Cerebral angioendotheliomatosis. Arch Pathol Lab Med 1982;106:342–6.
Bhawan J, Wolff SM, Ucci AA, et al. Malignant lymphoma and malignant angioendotheliomatosis: one disease. Cancer 1985;55:570–6.
Dominguez FE, Rosen LB, Kramer HC. Malignant angioendotheliomatosis proliferans. Am J Dermatopathol 1986;8:419–25.
Sheibani K, Battifora H, Winberg CD, et al. Further evidence that “malignant angioendotheliomatosis” is an angiotropic large-call lymphoma. N Engl J Med 1986;314:943–8.
Willemze R, Kroyswijk MRJ, Debruin CD, et al. Angiotropic (intravascular) large cell lymphoma of the skin previously classified as malignant angioendotheliomatosis. Br J Dermatol 1987;116:393–9.
Wrotnowski U, Mills SE, Cooper PH. Malignant angioendotheliomatosis. An angiotropic lymphoma. Am J Clin Pathol 1985;83:244–8.
Wick MR, Mills SE, Scheithauer BW, et al. Reassessment of malignant “angioendotheliomatosis:” evidence in favor of its reclassification as “intravascular lymphomatosis.” Am J Surg Pathol 1986;10:112–3.
Fulling KH, Gersell DJ. Neoplastic angioendotheliomatosis: histologic, immunohistochemical, and ultrastructural findings in two cases. Cancer 1982;51:1107–18.
Carroll TJ, Schelper RL, Goeken JA, et al. Neoplastic angioendotheliomatosis: immunopathologic and morphologic evidence for intravascular malignant lymphomatosis. Am J Clin Pathol 1986;85:169–75.
Mori S, Itoyama S, Mohri N, et al. Cellular characteristics of neoplastic angioendotheliomatosis. An immunohistochemical marker study of 6 cases. Virchows Arch Pathol Anat 1985;407:167–75.
Ferry JA, Harris NL, Picker LJ, et al. Intravascular lymphomatosis (malignant angioendotheliomatosis). A B-cell neoplasm expressing surface homing receptor. Mod Pathol 1988;1:444–52.
Otrakji CL, Voight W, Amador A, et al. Malignant angioendotheliomatosis: a true lymphoma. A case of intravascular malignant lymphomatosis studied by Southern blot hybridization analysis. Hum Pathol 1988;19:475–8.
Bhawan J. Angioendotheliomatosis proliferans systemisata: an angiotropic neoplasm of lymphoid origin. Semin Diagn Pathol 1987;4:18–27.
Petroff N, Koger OW, Fleming MG, et al. Malignant angioendotheliomatosis: an angiotropic lymphoma. J Am Acad Dermatol 1989;21:727–33.
Molina A, Lombard C, Donlon T, Bangs CD, Dorfman RF. Immunohistochemical and cytogenetic studies indicate that malignant angioendotheliomatosis is a primary intravascular (angiotropic) lymphoma. Cancer 1990;66:474–9.
Sepp N, Schuler G, Romani N, et al. “Intravascular lymphomatosis” (angioendotheliomatosis): evidence for a T-cell origin in two cases. Hum Pathol 1990;21:1051–8.
Hisashi T, Tadaaki E, Toyohiro T, Masuzou K, Yokio F, Syouji K. Congenital angiotropic lymphoma (intravascular lymphomatosis) of the T-cell type. Cancer 1991;67:2131–6.
Kitagawa M, Matsubara 0, Song SY, et al. Neoplastic angioendotheliomatosis. Immunohistochemical and electron microscopic findings in three cases. Cancer 1985;56:1134–43.
Petito CK, Gottlieb GJ, Dougherty JH, et al. Neoplastic angioendotheliomatosis: Ultrastructural study and review of the literature. Ann Neurol 1978;3:393–9.
Keahey TM, Guerry D IV, Tuthill RJ, Bondi EE. Malignant angioendotheliomatosis prolifeerans treated with doxorubicin. Arch Dermatol 1982;118:512–4.
Setoyama M, Mizoguchi S, Orikawa T, Tashiro M. A case of intravascular malignant lymphomatosis (angiotropic large-cell lymphoma) presenting memory T-cell phenotype and its expression of adhesion molecules. J Dermatol 1992;19:263–9.
Sangueza O, Hyder DM, Sangueza P. Intravascular lymphomatosis: report of an unusual case with T-cell phenotype occurring in an adolescent male. J Cutan Pathol 1992;19:226–31.
Kamesaki H, Matsui Y, Ohno Y, et al. Single case report: angiocentric lymphoma with histologic features of neoplastic angioendotheliomatosis presenting with predominant respiratory and hematologic manifestations. Am J Clin Pathol 1990;94:768–72.
Rubin MA, Cossman J, Freter CE, Azumi N. Intravascular large cell lymphoma coexisting within hemangiomas of the skin. Am J Surg Pathol 1997;21:860–4.
Ramsay B, Dahl MGC, Malcolm AJ, Soyer HP, Wilson Jones E. Acral pseudolymphomatous angiokeratoma of children (APACHE). Br J Dermatol 1988;119(suppl 33):13.
Ramsay B, Dahl MGC, Malcolm AJ, Wilson Jones E. Acral pseudolymphomatous angiokeratoma of children. Arch Dermatol 1990:126:1524–5.
Hara M, Matsunaga J, Tagami H. Acral pseudolymphomatous angiokeratoma of children (APACHE): a case report and immunohistologic study. Br J Dermatol 1991;124:387–8.
Kaddu S, Cerroni L, Pilatti A, Soyer HP, Kerl H. Acral pseudolymphomatous angiokeratoma. A variant of cutaneous pseudolymphomas. Am J Dermatopathol 1994;16:130–3.
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2003 Springer Science+Business Media New York
About this chapter
Cite this chapter
Sangüeza, O.P., Requena, L. (2003). Disorders Erroneously Considered as Vascular Neoplasms. In: Pathology of Vascular Skin Lesions. Current Clinical Pathology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-360-6_11
Download citation
DOI: https://doi.org/10.1007/978-1-59259-360-6_11
Publisher Name: Humana Press, Totowa, NJ
Print ISBN: 978-1-61737-407-4
Online ISBN: 978-1-59259-360-6
eBook Packages: Springer Book Archive