Neuroendocrine differentiation in 32 cases of so-called sclerosing hemangioma of the lung: identified by immunohistochemical and ultrastructural study.

Thirty-two cases of so-called sclerosing hemangioma of the lung observed by light microscopy were further studied by electron microscopy and/or immunohistochemistry. Three histologic patterns were seen: hemangioma-like, papillary, and solid. The only significant component representing the nature of the lesion is characteristic round cells within the stroma in all these patterns, whereas the surface cells lining the papillary projections or cystic spaces are normal or are hyperplastic bronchioloalveolar cells with a few neuroendocrine cells. Immunohistochemical findings showed that the "stromal cells" (tumor cells) were positive for neuroendocrine markers, namely, chromogranin A (19 of 22 cases), neuron-specific enolase (24 of 24), synaptophysin (six of 10), adrenocorticotropic hormone (14 of 15), growth hormone (14 of 15), calcitonin (11 of 15), and gastrin (11 of 14). Besides, some tumor cells were positive for epithelial membrane antigen (four of four), carcinoembryonic antigen (one of four), and vimentin (one of one). All tumor cells were negative for polyclonal antikeratin antibody (25 cases), AE1 (one case), and AE3 (one case). However, in contrast to the "stromal cells," the surface cells of the cystic spaces stained positively for keratin (25 of 25 cases), AE1 (one of one), AE3 (one of one), epithelial membrance antigen (four of four), and carcinoembryonic antigen (four of four); only a few of them expressed neruoendocrine markers. Both surface and tumor cells were negative for factor VIII-related antigen (25 cases), CD31 (one case), and alpha1-antitrypsin (25 cases). Ten cases further studied by electron microscopy and six examined by ultrastructural morphometry showed that the surface cells were mainly type 2 pneumocytes containing many lamellar bodies in the cytoplasm. Lying among them, neuroendocrine cells were occasionally seen. The stromal tumor cells had no lamellar body, but dense core granules (neurosecretory granules) and microtubules. In six cases, 92.3% (345 of 374) of tumor cells contained neurosecretory granules, which were pleomorphic and 73 to 1056 nm in diameter (mean, 302 nm). Two to 193 (mean, 12) neurosecretory granules were found in each tumor cell. Both immunohistochemical findings and ultrastructural evidence indicate that so-called sclerosing hemangioma of the lung is a benign lesion composed of neoplastic neuroendocrine cells with areas of sclerosis. A suggested name for this tumor is benign neuroendocrine tumor of the lung. The differentiation between this tumor and papillary adenoma, bronchioloalveolar carcinoma, or carcinoid tumor of the lung is discussed.

[1]  J. Rosai,et al.  Diffuse idiopathic pulmonary neuroendocrine cell proliferation presenting as interstitial lung disease. , 1995, The American journal of surgical pathology.

[2]  K. Chan,et al.  A morphological and immunohistochemical study of 25 cases of so‐called sclerosing haemangioma of the lung , 1995, Histopathology.

[3]  H. Xu,et al.  [A benign neuroendocrine tumor of the lung: study on the origin of the so-called sclerosing hemangioma of the lung]. , 1994, Zhonghua bing li xue za zhi = Chinese journal of pathology.

[4]  P. Heikkilä,et al.  Papillary pneumocytoma of the lung. An immunohistochemical and electron microscopic study. , 1994, Pathology, research and practice.

[5]  A. Flint,et al.  Papillary adenoma of the lung. , 1992, American journal of clinical pathology.

[6]  K. Sueishi,et al.  Sclerosing Hemangioma of the Lung: An Epithelial Tumor Composed of Immunohistochemically Heterogenous Cells , 1987 .

[7]  S. Suster,et al.  Sclerosing hemangioma of the lung. Immunohistochemical demonstration of mesenchymal origin using antibodies to tissue‐specific intermediate filaments , 1986, Cancer.

[8]  H. Spencer,et al.  Sclerosing haemangiomas of the lung , 1986, Histopathology.

[9]  T. Naruke,et al.  Papillary adenoma of type 2 pneumocytes. , 1986, The American journal of surgical pathology.

[10]  A. Katzenstein,et al.  So‐called sclerosing hemangioma of the lung: Evidence for mesothelial origin , 1983, The American journal of surgical pathology.

[11]  K. Geisinger,et al.  Papillary adenoma of the lung with lamellar and electron dense granules an ultrastructural study , 1982 .

[12]  E. Álvarez-Fernández,et al.  Sclerosing haemangioma of the lung. A histochemical, electron microscopical, tissue culture and time‐lapse cinematographic study , 1981, Histopathology.

[13]  E. Mark,et al.  Papillary carcinoid tumor of the lung , 1981, Cancer.

[14]  S. Hsu,et al.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. , 1981, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[15]  C. Carrington,et al.  Sclerosing hemangioma of the lung: A clinicopathologic study of 51 cases , 1980, The American journal of surgical pathology.

[16]  P. M. Escribano,et al.  Sclerosing hemangioma of the lung An ultrastructural study , 1979, Cancer.

[17]  D. Borochovitz,et al.  Sclerosing hemangioma of the lung: an endothelial or epithelial neoplasm? , 1977, Human pathology.

[18]  S. Nair,et al.  Fibrous histiocytoma of the lung (sclerosing hemangioma variant?). , 1974, Chest.

[19]  G. Hill,et al.  Electron microscopic study of so called “pulmonary sclerosing hemangioma”.Report of a case suggesting epithelial origin , 1972, Cancer.

[20]  J. Haas,et al.  Ultrastructure of a sclerosing hemangioma of the lung , 1972, Cancer.

[21]  S. Mills,et al.  So-called sclerosing hemangiomas of lung. An immunohistochemical study supporting a respiratory epithelial origin. , 1988, The American journal of surgical pathology.

[22]  K. Sueishi,et al.  Sclerosing hemangioma of the lung. Immunohistochemical characterization of its origin as related to surfactant apoprotein , 1985, Cancer.

[23]  A. Liebow,et al.  Sclerosing hemangioma (histiocytoma, xanthoma) of the lung , 1956, Cancer.