Skip to main content

Pulmonary Histiocytosis X (Pulmonary Langerhans’ Cell Granulomatosis)

  • Chapter
Pulmonary Pathology

Abstract

A conceptual understanding of pulmonary histiocytosis X, also known as pulmonary eosinophilic granuloma and pulmonary Langerhans’ cell granulomatosis, is based on a knowledge of the Langerhans’ cell. The Langerhans’ cell was named after Paul Langerhans, a 24-year-old German medical student who identified it as a dendritic cell of the epidermis of uncertain origin and function.1 He thought these cells represented nerve cells. In 1961, Birbeck et al.2 discovered by electron microscopy that Langerhans’ cells contained unique rod- and racquet-shaped granules that are now referred to as Langerhans’ cell granules or Birbeck granules. In 1965, Basset and Turiaf3 found that histiocytosis X cells contained the same type of unusual cytoplasmic granule that was found in Langerhans’ cells, and called them histiocytosis X bodies or X bodies. Langerhans’ cells and histiocytosis X cells are bone marrow derived4,5 and have features similar but not identical to those of monocytes and macrophages6–13; these are shown in Table 17-1. More recent studies have shown that Langerhans’ cells belong to a specific subset of macrophages, termed dendritic cells or antigen-presenting cells.14,15 In 1986, Murphy and coworkers16 demonstrated, in skin biopsies from patients who had undergone bone marrow transplantation, that phagocytic dermal macrophages transform into Langerhans’ cells. Langerhans’ cells are stated to reach normal levels 4 to 12 months after transplantation.17

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 74.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Similar content being viewed by others

References

  1. Langerhans P. Uber die Nerven der menschlichen Haut. Virchows Arch [Pathol Anat] 1868; 44: 325–337.

    Article  Google Scholar 

  2. Birbeck MS, Breathnach AD, Everall JD. An electron microscope study of basal melanocytes and high-level clear cells (Langerhans cells) in vitiligo. J Invest Dermatol 1961; 37: 51–64.

    Google Scholar 

  3. Basset F, Turiaf J. Identification par la microscopie electronique de particles de nature probablement virale dans les lesions granulomateuses d’une histiocytose X pulmonaire. CR Seances Acad Sci (Paris) 1965; 261: 3701–3703.

    CAS  Google Scholar 

  4. Katz SI, Tamaki K, Sachs DH. Epidermal Langerhans cells are derived from cells originating in bone marrow. Nature (London) 1979; 282: 324–326.

    Article  CAS  Google Scholar 

  5. Wood GS, Morhenn VB, Butcher EC, Kosek J. Langerhans cells react with panleukocyte monoclonal antibody. Ultrastructural documentation using a live cell suspension immunoperoxidase technique. J Invest Dermatol 1984; 82: 322–325.

    Article  PubMed  CAS  Google Scholar 

  6. Stingl G, Wolff-Schreiner EC, Pichler WJ, Gschnait F, Knapp W. Epidermal Langerhans cells bear Fc and C3 receptors. Nature (London) 1977; 268: 245–246.

    Article  CAS  Google Scholar 

  7. Rowden G, Lewis MC, Sullivan AK. Ia antigen expression on human Langerhans cells. Nature (London) 1977; 268: 247–248.

    Article  CAS  Google Scholar 

  8. Murphy GF, Bhan AK, Sato S, Harrist JJ, Mihm MC. Characterization of Langerhans cells by the use of monoclonal antibodies. Lab Invest 1981; 45: 465–468.

    PubMed  CAS  Google Scholar 

  9. Favara BE, McCarthy RC, Mierau GW. Histiocytosis X. Hum Pathol 1983; 14: 663–676.

    Article  PubMed  CAS  Google Scholar 

  10. Beckstead JH, Wood GS, Turner RR. Histiocytosis X cells and Langerhans cells: enzyme histochemical and immunologic similarities. Hum Pathol 1984; 15: 826833.

    Google Scholar 

  11. Takahashi K, Isobe T, Ohtsuki Y, Sonobe H, Takeda I, Akagi T. Immunohistochemical localization and distribution of S-100 protein in human lymphoreticular system. Am J Pathot 1984; 116: 497–503.

    CAS  Google Scholar 

  12. Wood GS, Turner RR, Shiurba RA, Eng L, Warnke RA. Human dendritic cells and macrophages: in situ immunophenotypic definition of subsets that exhibit specific morphologic and microenvironmental characteristics. Am J Pathol 1985; 119: 73–82.

    PubMed  CAS  Google Scholar 

  13. Franklin WA, Mason DY, Pulford K, et al. Immunohistologic analysis of human mononuclear phagocytes and dendritic cells by using monoclonal antibodies. Lab Invest 1986; 54: 322–335.

    PubMed  CAS  Google Scholar 

  14. Rochester CL, Goodell EM, Stoltenborg JK, Bowers WE. Dendritic cells from rat lung are potent accessory cells. Am Rev Respir Dis 1988; 138: 121–128.

    Article  PubMed  CAS  Google Scholar 

  15. Toews GB. Pulmonary dendritic cells: Sentinels of lung-associated lymphoid tissues. Am J Respir Cell Mol Biol 1991; 4: 204–205.

    Article  PubMed  CAS  Google Scholar 

  16. Murphy GF, Messadi D, Fonferko I, Hancock WW. Phenotypic transformation of macrophages to Langerhans cells in the skin. Am J Pathol 1986; 123: 401–406.

    PubMed  CAS  Google Scholar 

  17. Komp DM. Langerhans cell histiocytosis. N Engl J Med 1987; 316: 747–748.

    Article  PubMed  CAS  Google Scholar 

  18. Hammar S. Langerhans cells. Path Ann 1988 (Part 2); 23: 293–328.

    Google Scholar 

  19. Hammar S, Bockus D, Remington F, Bartha M. The widespread distribution of Langerhans’ cells in pathologic conditions: An ultrastructural and immunohistochemical study. Hum Pathol 1986; 17: 894–905.

    Article  PubMed  CAS  Google Scholar 

  20. Farber S. The nature of “solitary or eosinophilic granuloma” of bone. Am J Pathol 1941; 17: 625.

    Google Scholar 

  21. Lichtenstein L. Histiocytosis X. Integration of eosinophilic granuloma of bone. “Letterer-Siwe disease” and “Schuller-Christian disease” as related manifestations of a single nosologic entity. Arch Pathol Lab Med 1953; 56: 84–102.

    CAS  Google Scholar 

  22. Lieberman P, Jones C, Dargeon H, Begg CF. A reappraisal of eosinophilic granuloma of bone, HandSchuller-Christian syndrome and Letterer-Siwe syndrome. Medicine (Baltimore) 1969; 48: 375–400.

    CAS  Google Scholar 

  23. Vogel JM, Vogel P. Idiopathic histiocytosis: a discussion of eosinophilic granuloma, the Hand-Schuller-Christian syndrome and the Letterer-Siwe syndrome. Semin Hematol 1972; 9: 349–369.

    PubMed  CAS  Google Scholar 

  24. Lewis JG. Eosinophilic granuloma and its variants with special reference to lung involvement. A report of 12 patients. Q J Med 1964; 33: 337–359.

    Google Scholar 

  25. Parkinson T. Eosinophilic xanthomatous granuloma with honeycomb lungs. Br Med J 1949; 1: 1029–1030.

    Article  PubMed  CAS  Google Scholar 

  26. Oswald N, Parkinson T. Honeycomb lungs. Q J Med 1949; 18: 1–20.

    PubMed  CAS  Google Scholar 

  27. Cunningham GJ, Parkinson T. Diffuse cystic lungs of granulomatous origin. A histological study of six cases. Thorax 1950; 5: 43–58.

    Article  Google Scholar 

  28. Farinacci CJ, Jeffrey HC, Lackey RW. Eosinophilic granuloma of the lung. Report of two cases. US Armed Forces Med J 1951; 2: 1085–1093.

    CAS  Google Scholar 

  29. Mazitello WF. Eosinophilic granuloma of the lung. N Engl J Med 1954; 250: 804–809.

    Article  Google Scholar 

  30. Basset F, Corrin B, Spencer H, et al. Pulmonary histiocytosis X. Am Rev Respir Dis 1978; 118: 811–820.

    PubMed  CAS  Google Scholar 

  31. Friedman PJ, Liebow AA, Sokoloff J. Eosinophilic granuloma of lung: clinical aspects of primary pulmonary histiocytosis in the adult. Medicine (Baltimore) 1981; 60: 385–396.

    Article  CAS  Google Scholar 

  32. Hammar SP, Hallman KO, Winterbauer RH, et al. Primary pulmonary histiocytosis X: A clinicopathologic analysis of 31 patients.

    Google Scholar 

  33. Colby TV, Lombard C. Histiocytosis X in the lung. Hum Pathol 1983; 14: 847–856.

    Article  PubMed  CAS  Google Scholar 

  34. Villar TG, Avila R, Marques RA. Eosinophilic granuloma of the lung and the extrinsic pulmonary granulomatoses. Ann NY Acad Sci 1976; 278: 612–617.

    Article  PubMed  CAS  Google Scholar 

  35. Girard P, Bouzakoura C. Eosinophilic granuloma of the lung with sawdust and horse serum hypersensitivity. Clin Allergy 1974; 4: 71–78.

    Article  PubMed  CAS  Google Scholar 

  36. Auld D. Pathology of eosinophilic granuloma of lung. Arch Pathol Lab Med 1957; 63: 113–131.

    CAS  Google Scholar 

  37. Thompson JR, Langer S. Eosinophilic granuloma of the lungs. Dis Chest 1964; 46: 553–561.

    Article  PubMed  CAS  Google Scholar 

  38. King TE, Schwarz MI, Dreisin RE, Pratt DS, Theofilopoulos AN. Circulating immune complexes in pulmonary eosinophilic granuloma. Ann Intern Med 1979; 91: 397–399.

    Article  PubMed  Google Scholar 

  39. Dreisen RB, Schwarz MI, Theofilopoulous AN, Stanford RE. Circulating immune complexes in the idiopathic interstitial pneumonias. N Engl J Med 1978; 298: 353–357.

    Article  Google Scholar 

  40. Haslam PM. Circulating immune complexes in patients with cryptogenic fibrosing alveolitis. Clin Exp Immunol 1979; 37: 381–390.

    PubMed  CAS  Google Scholar 

  41. Ahnquist G, Holyoke JB. Congenital Letterer-Siwe disease (reticuloendotheliosis) in a term stillborn infant. J Pediatr 1960; 57: 897–904.

    Article  PubMed  CAS  Google Scholar 

  42. Claman HN, Suvatte V, Githens JH, Hathaway WE. Histiocytic reaction in dysgammaglobulinemia and congenital rubella. Pediatrics 1970; 46: 89–96.

    PubMed  CAS  Google Scholar 

  43. van der Loo FM, van Muijen GNP, van Vloten WA, Beens W, Scheffer F, Meijer CJLM. C-type virus-like particles specifically localized in Langerhans cells and related cells of skin and lymph nodes of patients with mycosis fungoides and Sezary syndrome. Virchows Arch [Cell Pathol] 1979; 31: 193–203.

    Article  Google Scholar 

  44. Osband ME, Lipton JM, Lavin P, et al. Histiocytosis X: demonstration of abnormal immunity, T-cell histamine H2-receptor deficiency and successful treatment with thymic extract. N Engl J Med 1981; 304: 146–153.

    Article  PubMed  CAS  Google Scholar 

  45. Miller LG, Goldstein G, Murphy M, Ginns LC. Reversible alterations in immunoregulatory T cells in smoking: Analysis by monoclonal antibodies and flow cytometry. Chest 1982; 82: 526–529.

    Article  PubMed  CAS  Google Scholar 

  46. Gerard JW, Heiner PC, Mink J, Meyers A, Dosman JA. Immunoglobulin levels in smokers and non-smokers. Ann Allergy 1980; 44: 261–262.

    Google Scholar 

  47. Ferson M, Edwards A, Lind A, Milton GW, Hersey P. Low natural killer-cell activity and immunoglobulin levels associated with smoking in human subjects. Int J Cancer 1979; 23: 603–609.

    Article  PubMed  CAS  Google Scholar 

  48. Cryer PE, Haymond MW, Santiago JV, Shah SD. Norepinephrine and epinephrine release and adrenergic mediation of smoking-associated hemodynamic and metabolic events. N Engl J Med 1976; 295: 573–577.

    Article  PubMed  CAS  Google Scholar 

  49. Miller CL, Baker CC. Changes in lymphocyte activity after injury. J Clin Invest 1977; 63: 202–210.

    Article  Google Scholar 

  50. Wang BS, Heacock EH, Wu AV, Mannick JA. Generation of suppressor cells in mice after surgical trauma. J Clin Invest 1980; 66: 200–209.

    Article  PubMed  CAS  Google Scholar 

  51. Hoogsteden HC, van Hal PThW, Wijkhuijs JM, Hop W, Verkaik APK, Hilvering C. Expression of the CD11/ CD18 cell surface adhesion glycoprotein family on alveolar macrophages in smokers and nonsmokers. Chest 1991; 100: 1567–1571.

    Article  PubMed  CAS  Google Scholar 

  52. Senior RM, Kuhn C, III. The pathogenesis of emphysema. In: Fishman AP, ed. Pulmonary diseases and disorders. 2d Ed. New York: McGraw-Hill, 1988; 2: 1209–1219.

    Google Scholar 

  53. Kasama T, Kobayashi K, Fukushima T, et al. Production of interleukin 1-like factor from human peripheral blood monocytes and polymorphonuclear leukocytes by superoxide anion: The role of interleukin 1 and reactive oxygen species in inflamed sites. Clin Immunol Immunopathol 1989; 53: 439–448.

    Article  PubMed  CAS  Google Scholar 

  54. Renoux M, Lemarié E, Renoux G. Interleukin-1 secretion by lipopolysaccharide-stimulated alveolar macrophages. Respiration 1989; 55: 158–168.

    Article  PubMed  CAS  Google Scholar 

  55. Rothlein R, Czajkowski M, O’Neill MM, Marlin SD, Mainolfi E, Merluzzi VJ. Induction of intercellular adhesion molecule 1 on primary and continuous cell lines by pro-inflammatory cytokines: Regulation by pharmacologic agents and neutralizing antibodies. J Immunol 1988; 141: 1665–1669.

    PubMed  CAS  Google Scholar 

  56. Barbers RG, Evans MJ, Gong H, Jr., Tashkin DP. Enhanced alveolar monocytic phagocyte (macrophage) proliferation in tobacco and marijuana smokers. Am Rev Respir Dis 1991; 143: 1092–1095.

    Article  PubMed  CAS  Google Scholar 

  57. Coggle JE, Tarling JD. The proliferation kinetics of pulmonary alveolar macrophages. J Leukocyte Biol 1984; 35: 317–327.

    PubMed  CAS  Google Scholar 

  58. Bitterman PB, Saltzman LE, Adelberg S, Ferrans VJ, Crystal RG. Alveolar macrophage replication. One mechanism for the expansion of the mononuclear phagocyte population in the chronically inflamed lung. J Clin Invest 1984; 74: 460–469.

    Article  PubMed  CAS  Google Scholar 

  59. Evans MJ, Sherman MP, Campbell LA, Shami SG. Proliferation of pulmonary alveolar macrophages during postnatal development of rabbit lungs. Am Rev Respir Dis 1987; 136: 384–387.

    Article  PubMed  CAS  Google Scholar 

  60. Evans MJ, Shami SG, Martinez LA. Enhanced proliferation of pulmonary macrophages after carbon instillation in mice depleted of blood monocytes by strontium-89. Lab Invest 1986; 54: 154–159.

    PubMed  CAS  Google Scholar 

  61. Blusse Van OudAlblas A, VanFurth R. Origin, kinetics and characteristics of pulmonary macrophages in the normal steady state. J Exp Med 1979; 149: 1504–1518.

    Article  Google Scholar 

  62. Shellito J, Esparza C, Armstrong C. Maintenance of the normal rat alveolar macrophage cell population. The roles of monocyte influx and alveolar macrophage proliferation in situ. Am Rev Respir Dis 1987; 135: 78–82.

    PubMed  CAS  Google Scholar 

  63. Golde DW, Byers LA, Finley TN. Proliferative capacity of human alveolar macrophages. Nature (London) 1974; 247: 373–375.

    Article  CAS  Google Scholar 

  64. Sawyer RT. The significance of local resident pulmonary alveolar macrophages in monocytopenic mice. J Leukocyte Biol 1986; 39: 77–87.

    PubMed  CAS  Google Scholar 

  65. Sherman MP, Evans MJ, Campbell LA. Prevention of pulmonary alveolar macrophage proliferation in newborn rabbits by hyperoxia. J Pediatr 1988; 112: 782–786.

    Article  PubMed  CAS  Google Scholar 

  66. Barbers RG, Oishi J, Gong H, Jr., Tashkin DP, Wallace JM, Baker SS. Chemotaxis of peripheral blood and lung leukocytes obtained from tobacco and marijuana smokers. J Psychoact Drugs 1988; 20: 15–20.

    Article  CAS  Google Scholar 

  67. Tashkin DP, Coulson AH, Clark VA, et al. Respiratory symptoms and lung function in habitual heavy smokers of marijuana alone, smokers of marijuana and tobacco, smokers of tobacco alone, and nonsmokers. Am Rev Respir Dis 1988; 138: 74–80.

    Article  Google Scholar 

  68. Hunninghake GW, Crystal RG. Cigarette smoking and lung destruction. Am Rev Respir Dis 1983; 128: 873–878.

    Google Scholar 

  69. Aguayo SM, Kane MA, King TE, Jr., Schwarz MI, Graver L, Miller YE. Increased levels of bombesin-like peptides in the lower respiratory tract of asymptomatic cigarette smokers. J Clin Invest 1989; 84: 1105–1113.

    Article  PubMed  CAS  Google Scholar 

  70. Aguayo SM, King TE, Jr., Waldron JA, Sherritt KM, Kane MA, Miller YE. Increased pulmonary neuroendocrine cells with bombesin-like immunoreactivity in adult patients with eosinophilic granuloma. J Clin Invest 1990; 86: 838–844.

    Article  PubMed  CAS  Google Scholar 

  71. Barth J, Kreipe H, Radzun HJ, et al. Increased expression of growth factor genes for macrophages and fibroblasts in bronchoalveolar lavage cells of a patient with pulmonary histiocytosis X. Thorax 1991; 46: 835–838.

    Article  PubMed  CAS  Google Scholar 

  72. Knudson RJ, Badger TL, Gaensler EA. Eosinophilic granuloma of lung. Med Thorac 1966; 23: 248–262.

    PubMed  CAS  Google Scholar 

  73. Guardia J, Pedreira J, Esteban R, Vargas V, Allende E. Early pleural effusion in histiocytosis X. Arch Intern Med 1979; 139: 934–936.

    Article  PubMed  CAS  Google Scholar 

  74. Masson RG, Tedeschi LG. Pulmonary eosinophilic granuloma with hilar adenopathy simulating sarcoidosis. Chest 1978; 73: 682–683.

    Article  PubMed  CAS  Google Scholar 

  75. Brambilla E, Fontaine E, Pison CM, Coulomb M, Paramelle B, Brambilla C. Pulmonary histiocytosis X with mediastinal lymph node involvement. Am Rev Respir Dis 1990; 142: 1216–1218.

    Article  PubMed  CAS  Google Scholar 

  76. Pomeranz SJ, Proto AV. Histiocytosis X. Unusual-confusing features of eosinophilic granuloma. Chest 1986;89:88–92.

    Google Scholar 

  77. Fichtenbaum CJ, Kleinman GM, Haddad RG. Eosinophilic granuloma of the lung presenting as a solitary pulmonary nodule. Thorax 1990; 45: 905–906.

    Article  PubMed  CAS  Google Scholar 

  78. Sajjad SM, Luna MA. Primary pulmonary histiocytosis X in two patients with Hodgkin’s disease. Thorax 1982; 37; 110–113.

    Article  PubMed  CAS  Google Scholar 

  79. Wyre HW, Henrichs WD. Systemic mastocytosis and pulmonary eosinophilic granuloma. JAMA 1978; 239: 856–857.

    Article  PubMed  Google Scholar 

  80. Shanley DJ, Lerud KS, Luetkehans TJ. Development of pulmonary histiocytosis X after chemotherapy for Hodgkin disease. AJR 1990; 155: 741–742.

    Article  PubMed  CAS  Google Scholar 

  81. Coli A, Bigotti G, Ferrone S. Histiocytosis X arising in Hodgkin’s disease: Immunophenotypic characterization with a panel of monoclonal antibodies. Virchows Arch A Pathol Anat 1991; 418: 369–373.

    Article  CAS  Google Scholar 

  82. LaCronique J, Roth C, Battesti JP, Basset F, Chretien J. Chest radiological features of pulmonary histiocytosis X. A report based on 50 adult cases. Thorax 1982; 37: 104–109.

    Article  PubMed  CAS  Google Scholar 

  83. Moor ADA, Godwin JD, Müller NL, et al. Pulmonary histiocytosis X: Comparison of radiographic findings. Radiology 1989; 172: 249–254.

    Google Scholar 

  84. Taylor DB, Joske D, Anderson J, Barry-Walsh C. Cavitating pulmonary nodules in histiocytosis X: High resolution CT demonstration. Aust Radiol 1990; 34: 253–255.

    Article  CAS  Google Scholar 

  85. Bedrossian CWM, Kuhn C III, Luna MA, Conklin RH, Byrd RB, Kaplan PD. Desquamative interstitial pneumonia-like reaction accompanying pulmonary lesions. Chest 1977; 72: 166–169.

    Article  PubMed  CAS  Google Scholar 

  86. Fukuda Y, Basset F, Soler P, Ferrans V, Masugi Y, Crystal RG. Intraluminal fibrosis and elastic fiber degradation lead to lung remodeling in pulmonary Langerhans cell granulomatosis (histiocytosis X). Am J Pathol 1990; 137: 415–424.

    PubMed  CAS  Google Scholar 

  87. Askin FB, McCann BG, Kuhn C III. Reactive eosinophilic pleuritis. A lesion to be distinguished from pulmonary eosinophilic granuloma. Arch Pathol Lab Med 1977; 101: 187–191.

    PubMed  CAS  Google Scholar 

  88. Hammar SP, Winterbauer RH, Bockus D, Remington F, Friedman S. Idiopathic fibrosing alveolitis: a review with emphasis on ultrastructural and immunohistochemical features. Ultrastruct Pathol 1985; 9: 345–372.

    Article  PubMed  CAS  Google Scholar 

  89. Hammar SP, Bolen JW, Bockus D, Remington F, Friedman S. Ultrastructural and immunohistochemical features of common lung tumors. An overview. Ultrastruct Pathol 1985; 9: 283–318.

    Article  CAS  Google Scholar 

  90. Hammar SP, Bockus D, Remington F, et al. Langerhans cells and serum precipitating antibodies against fungal antigen in bronchiolo-alveolar cell carcinomas: possible association with eosinophilic granuloma. Ultrastruct Pathol 1980; 1: 19–37.

    Article  PubMed  CAS  Google Scholar 

  91. Lombard CM, Medeiros J, Colby TV. Pulmonary histiocytosis X and carcinoma. Arch Pathol Lab Med 1987; 111: 339–341.

    PubMed  CAS  Google Scholar 

  92. Sadoun D, Vaylet F, Valeyre D, et al. Bronchogenic carcinoma in patients with pulmonary histiocytosis X. Chest 1992; 101: 1610–1613.

    Article  PubMed  CAS  Google Scholar 

  93. Tomasheski JF, Khiyami A, Kleinerman J. Neoplasms associated with pulmonary eosinophilic granuloma. Arch Pathol Lab Med 1991; 115: 499–506.

    Google Scholar 

  94. Wall CP, Gaensler EA, Carrington CB, Hayes JA. Comparison of transbronchial and open biopsies in chronic infiltrative lung disease. Am Rev Respir Dis 1981; 123: 280–290.

    PubMed  CAS  Google Scholar 

  95. Flint A, Lloyd RV, Colby TV, Wilson BW. Pulmonary histiocytosis X: Immunoperoxidase staining for HLA-DR antigen and S100 protein. Arch Pathol Lab Med 1986; 110: 930–933.

    PubMed  CAS  Google Scholar 

  96. Ree HJ, Kadin ME. Peanut agglutinin: A useful marker for histiocytosis X and interdigitating reticulum cells. Cancer (Philadelphia) 1986; 57: 282–287.

    Article  CAS  Google Scholar 

  97. Rabkin MS, Kjeldsberg CR. Epithelial membrane antigen staining patterns of histiocytic lesions. Arch Pathol Lab Med 1987; 111: 337–338.

    PubMed  CAS  Google Scholar 

  98. Azumi N, Sheibani K, Swartz WG, Stroup RM, Rappaport H. Antigenic phenotype of Langerhans cell histiocytosis: An immunohistochemical study demonstrating the value of LN-2, LN-3, and vimentin. Hum Pathol 1988; 19: 1376–1382.

    Article  PubMed  CAS  Google Scholar 

  99. Cagle PT, Mattioli CA, Truong LD, Greenberg SD. Immunohistochemical diagnosis of pulmonary eosinophilic granuloma on lung biopsy. Chest 1988; 94: 1133–1137.

    Article  PubMed  CAS  Google Scholar 

  100. Santamaria M, Llamas L, Ree HJ, et al. Expression of silylated Leu-MI antigen in histiocytosis X. Am J Clin Pathol 1988; 89: 211–216.

    PubMed  CAS  Google Scholar 

  101. Ruco LP, Pulford KAF, Mason DY, et al. Expression of macrophage-associated antigens in tissues involved by Langerhans’ cell histiocytosis (histiocytosis X) Am J Clin Pathol 1989; 92: 273–279.

    PubMed  CAS  Google Scholar 

  102. Rabkin MS, Kjeldsberg CR, Wittwer CT, Marty J. A comparison study of two methods of peanut agglutinin staining with S100 immunostaining in 29 cases of histiocytosis X (Langerhans’ cell histiocytosis) Arch Pathol Lab Med 1990; 114: 511–515.

    PubMed  CAS  Google Scholar 

  103. Fe Y, Huang S, Dong H. Histiocytosis X: S-100 protein, peanut agglutinin, and transmission electron microscopic study. Am J Clin Pathol 1990; 94: 627–631.

    Google Scholar 

  104. Ornvold K, Ralfkiaer E, Carstensen H. Immunohistochemical study of the abnormal cells in Langerhans cell histiocytosis (histiocytosis X). Virchows Arch A Pathol Anat Histopathol 1990; 416: 403–410.

    Article  PubMed  CAS  Google Scholar 

  105. Kanitakis J, Fantini F, Pincelli C, Hermier C, Schmitt D, Thivolet J. Neuron-specific enolase is a marker of cutaneous Langerhans’ cell histiocytosis (“X”): A comparative study with S100 protein. Anticancer Res 1991; 11: 635–640.

    PubMed  CAS  Google Scholar 

  106. Baumal R, Kahn HJ, Marks A. Role of antibody to S100 protein in diagnostic pathology. Lab Invest 1988; 59: 152–153 (letter).

    Google Scholar 

  107. Webber D, Tron V, Askin F, Churg A. S-100 staining in the diagnosis of eosinophilic granuloma of lung. Am J Clin Pathol 1985; 84: 447–453.

    PubMed  CAS  Google Scholar 

  108. Soler P, Chollet S, Jacque C, Fukuda Y, Ferrans VJ, Basset F. Immunocytochemical characterization of pulmonary histiocytosis X cells in lung biopsies. Am J Pathol 1985; 118: 439–451.

    PubMed  CAS  Google Scholar 

  109. Chollet S, Soler P, Dournovo P, Richard MS, Ferrans VJ, Basset F. Diagnosis of pulmonary histiocytosis X by immunodetection of Langerhans cells in bronchoalveolar lavage fluid. Am J Pathol 1984; 115: 225–232.

    PubMed  CAS  Google Scholar 

  110. Averswald V, Barth J, Magnussen H. Value of CD-1positive cells in bronchoalveolar lavage fluid for the diagnosis of pulmonary histiocytosis X. Lung 1991; 169: 305–309.

    Article  Google Scholar 

  111. Hammar SP, Winterbauer RH, Bockus D. Diagnosis of eosinophilic granuloma by ultrastructural examination of sputum. Arch Pathol Lab Med 1978; 102: 606.

    PubMed  CAS  Google Scholar 

  112. Powers MA, Askin FB, Cresson DH. Pulmonary eosinophilic granuloma. A 25-year follow-up. Am Rev Respir Dis 1984; 129: 503–507.

    PubMed  CAS  Google Scholar 

  113. Ben-Ezra J, Bailey A, Azumi N, et al. Malignant histiocytosis X: A distinct clinicopathologic entity. Cancer (Philadelphia) 1991; 68: 1050–1060.

    Article  CAS  Google Scholar 

  114. Risdall RJ, Dehner LP, Duray P, Kobrinsky N, Robison L, Nesbit ME, Jr. Histiocytosis X (Langerhans’ cell histiocytosis): Prognostic role of histopathology. Arch Pathol Lab Med 1983; 107: 59–63.

    PubMed  CAS  Google Scholar 

  115. Goldberg N, Bauer K, Rosen ST, et al. Histiocytosis X flow cytometric DNA-content and immunohistochemical and ultrastructural analysis. Arch Dermatol 1986; 122: 446–450.

    Article  PubMed  CAS  Google Scholar 

  116. Rabkin MS, Wittwer CT, Kjeldsberg CR, Piepkorn MW. Flow-cytometric DNA content of histiocytosis X (Langerhans’ cell histiocytosis). Am J Pathol 1988; 131: 283–289.

    PubMed  CAS  Google Scholar 

  117. Ornvold K, Carstensen H, Larsen JK, Christensen J, Ralfkiaer E. Flow cytometric DNA analysis of lesions from 18 children with Langerhans cell histiocytosis (histiocytosis X). Am J Pathol 1990; 136: 1301–1307.

    PubMed  CAS  Google Scholar 

  118. Huhn D, Konig G, Weig J, Schneller W. Therapy in pulmonary histiocytosis X. Haematol Bluttransfus 1981; 27: 231–237.

    CAS  Google Scholar 

  119. Von Essen S, West W, Sitorius M, Rennard SI. Complete resolution of roentgenographic changes in a patient with pulmonary histiocytosis X. Chest 1990; 98: 765–767.

    Article  Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1994 Springer Science+Business Media New York

About this chapter

Cite this chapter

Hammar, S.P. (1994). Pulmonary Histiocytosis X (Pulmonary Langerhans’ Cell Granulomatosis). In: Dail, D.H., Hammar, S.P. (eds) Pulmonary Pathology. Springer, New York, NY. https://doi.org/10.1007/978-1-4757-3935-0_17

Download citation

  • DOI: https://doi.org/10.1007/978-1-4757-3935-0_17

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4757-3937-4

  • Online ISBN: 978-1-4757-3935-0

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics