Histiocytoses
DOI:
https://doi.org/10.66344/jpad.13.4.2003.761Abstract
Histiocytoses are an important group of dermatoses characterized by histological infiltrates predominantly rich in cells of monocyte-macrophage origin. The present review focuses on the salient clinical, diagnostic and therapeutic features of different entities included in this group.References
Glass AG, Miller RW. US mortality from Letterer-Siwe disease, 1960-1964. Pediatrics 1968; 42: 364-7.
McLelland J, Chu AC. Comparison of peanut agglutinin and S100 stain in the paraffin tissue diagnosis of Langerhans cell histiocytosis. Br J Dermatol 1988; 119: 513-21.
Rowden G, Connelly EM, Winkelmann R. Cutaneous histiocytosis X. The presence of S100 protein and its use in diagnosis. Arch Dermatol 1983; 119: 553-9.
McLelland J, Broadbent V, Yeoman E. Langerhans cell histiocytosis; a conservative approach to treatment. Arch Dis Child 1990; 65: 301-3.
de Berker D, Lever LR, Windebank K. Nail features in Langerhans cell histiocytosis. Br J Dermatol 1994; 130: 523-7.
Cunningham MJ, Curtin HD, Jaffe R. Otological manifestations of Langerhans cell histiocytosis. Arch Otolaryngol Head Neck Surg 1989; 115: 807-13.
Braunstein GD, Kohler PO. Endocrine manifestations of histiocytoses. Am J Pediatr Hematol Oncol 1981; 3: 67-75.
Wong E, Holden CA, Broadbent V. Histiocytosis X presenting as intertrigo and responding to topical nitrogen mustard. Clin Exp Dermatol 1986; 11: 183.
Broadbent V, Pritchard J, Yeoman E. Etoposide (VP16) in the treatment of multisystem Langerhans cell histiocytosis. Med Pediatr Oncol 1989; 17: 97-100.
McLelland J, Pritchard J, Chu AC. Current controversies. Hematol Oncol Clin North Am 1987; 1: 147-62.
Rodriguez J, Ackerman AB. Xanthogranuloma in adults. Arch Dermatol 1979; 112: 43-4.
Holde G, Bonsmann G. Generalized lichenoid juvenile xanthogranuloma. Br J Dermatol 1992; 120: 66-70.
MacLeod PM. Juvenile xanthogranuloma of the iris managed with superficial radiotherapy. Clin Radiol 1986; 37: 295-6.
Yee KC, Bowker CM, Tam CY. Cardiac and systemic complications in multicentric reticulohistiocytosis. Clin Exp Dermatol 1993; 18: 558-68.
Carey RN, Blotzer JW, Wolfe ID. Multicentric reticulohistiocytosis and Sjogren’s syndrome. J Rheumatol 1985; 12: 1193-5.
Snow JC, Muller SA. Malignancy associated histiocytoses: a clinical, histological and immunophenotypic study. Br J Dermatol 1995; 133: 71-6.
Kossard S, Winkelmann RK. Necrobiotic xanthogranuloma with paraproteinemia. J Am Acad Dermatol 1980; 3: 257-70.
Rosai J, Dorfmann RE. Sinus histiocytosis with massive lymphadenopathy: a pseudolymphomatous benign disorder. Analysis of 34 cases. Cancer 1972; 30: 1174-88.
Komatsuda A, Chubach A, Miura AB. Virus associated hemophagocytic syndrome due to measles accompanied by acute respiratory failure. Intern Med 1995; 34: 203-6.
Atlman J, Winklemann RK. Xanthoma disseminatum. Arch Dermatol 1962; 86: 582-9.
Calverly DC, Wismer J, Rosonthal D. Xanthoma disseminatum in an infant with skeletal and marrow involvement. J Pediatr Hematol Oncol 1995; 17: 61-5.
Blobstein SH, Caldwell D, Carter M. Bone lesions in xanthoma disseminatum. Arch Dermatol 1985; 121: 1313-7.
Finan MC, Winklemann RK. Necrobiotic xanthogranuloma with paraproteinemia. A review of 22 cases. Medicine 1986; 65: 376-88.
Warnke RM, Kim H, Dorfmann RE. Malignant histiocytoses (histiocytic medullary reticulosis). Clinicopathological study of 29 cases. Cancer 1975; 35: 215-30.
Ducatman BS, Wick MR, Morgan TW. Malignant histiocytosis: a clinical, histological and immunohistochemical study of 20 cases. Hum Pathol 1984; 15: 368-77.
Berry J, Russel JA. Salvage of relapsed malignant histiocytoses by autologous bone marrow transplantation. Bone Marrow Transplant 1989; 4: 123-4.
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