Literature DB >> 6412437

Giant cell granulomatosis of lymph nodes with a fatal course.

C Cozzutto, A Comelli, P G Mori, B De Bernardi.   

Abstract

We report two examples of an unusual expression of fatal granulomatosis with primary lymph node location, characterized histologically by numerous giant cells of the Langhans' type, effacement of the nodal structure, mixed lymphohistiocytic infiltrate, and marked histiocyte cell maturity, all features which initially did not exclude the possibility of a granulomatous process of infectious origin. The clinical features of these cases include cellular or combined immunodeficiency, a possible family history and a rapidly fatal course. The present article emphasizes the great similarity which can exist between histiocytic and granulomatous disorders, the great variability of histiocytic diseases from the pathological view-point, the presence of borderline examples, and the several overlapping features of different entities. Specifically, the most remarkable finding of these two cases is the existence of numerous mature giant cells of the Langerhans' type within a massive obliteration of the nodal structure. Furthermore, these giant cells characterized by a strikingly orderly disposition of peripheral nuclei in a wreath-like pattern, frequently suggesting the structure of Touton's giant cells.

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Mesh:

Year:  1983        PMID: 6412437     DOI: 10.1007/BF00612187

Source DB:  PubMed          Journal:  Virchows Arch A Pathol Anat Histopathol        ISSN: 0174-7398


  24 in total

1.  Malignant histiocytosis (histiocytic medullary reticulosis). I. Clinicopatholigic study of 29 cases.

Authors:  R A Warnke; H Kim; R F Dorfman
Journal:  Cancer       Date:  1975-01       Impact factor: 6.860

2.  An unusual acid-fast bacillus causing systemic disease and death in a child; with special reference to disseminated osteomyelitis and intracellular parasitism.

Authors:  L H VAN DER HOEVEN; F J RUTTEN; A VAN DER SAR
Journal:  Am J Clin Pathol       Date:  1958-05       Impact factor: 2.493

3.  Familial haemophagocytic reticulosis.

Authors:  J W FARQUHAR; A E CLAIREAUX
Journal:  Arch Dis Child       Date:  1952-12       Impact factor: 3.791

Review 4.  Histiocytosis X histogenetic arguments for a Langerhans cell origin.

Authors:  C Nezelof; F Basset; M F Rousseau
Journal:  Biomedicine       Date:  1973-09

Review 5.  [Reticulo-histiocytosis in children. Nosology and classification].

Authors:  C Nézelof
Journal:  Arch Fr Pediatr       Date:  1979-06

6.  Rapidly fatal familial histiocytosis associated with eosinophilia and primary immunological deficiency.

Authors:  R F Barth; G G Vergara; S K Khurana; J T Lowman; J B Beckwith
Journal:  Lancet       Date:  1972-09-09       Impact factor: 79.321

7.  Disseminated histiocytosis associated with atypical lymphoid cells (lymphohistiocytosis).

Authors:  C W Berard; R A Cooper; E J Freireich; A S Rabson
Journal:  Cancer       Date:  1966-10       Impact factor: 6.860

8.  Congenital hemophagocytic reticulosis.

Authors:  A Koto; R Morecki; M Santorineou
Journal:  Am J Clin Pathol       Date:  1976-04       Impact factor: 2.493

Review 9.  Lymphadenopathy as the initial manifestation of histiocytosis X.

Authors:  J W Williams; R F Dorfman
Journal:  Am J Surg Pathol       Date:  1979-10       Impact factor: 6.394

10.  Immunodeficiency in familial erythrophagocytic lymphohistiocytosis.

Authors:  S Ladisch; D G Poplack; B Holiman; R M Blaese
Journal:  Lancet       Date:  1978-03-18       Impact factor: 79.321

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