Literature DB >> 892791

Pulmonary angiitis and granulomatosis. The relationship between histological features, organ involvement, and response to treatment.

M J Saldana, A S Patchefsky, H I Israel, G W Atkinson.   

Abstract

The histologic findings, natural history, and response to treatment were investigated in 62 patients with pulmonary angiitis andgranulomatosis seen over a 23 year period. Three histologic types were recognized: lymphocyte depleted angiitis and granulomatosis, 24 cases (39 per cent); benign lymphocytic angiitis and granulomatosis, 14 cases (22 per cent); and malignant lymphoproiferative angiitis and granulomatosis, 24 cases (39 per cent). Lymphocyte depleted angiitis and granulomatosis corresponds to Wegener's granulomatosis of either the "limited" or "classic" variant. The lesions frequently show extensive liquefactive necrosis. Eosinophils may be abundant, but lymphocytes and plasma cells are relatively scarce. Histiocytic proliferation with the occasional presence of sarcoid-like granulomas was observed only in cases with no evidence of glomerular involvement. Cyclophosphamide is highly effective regardless of whether extrapulmonary manifestations are present. Benign lymphocytic angiitis and granulomatosis is characterized by dense benign infiltrates of lymphocytes, plasma cells, and histiocytes. Necrosis may be absent or minimal; the angiitis is usually mild to moderate. Only one of 14 patients (7 per cent) had extrapulmonary involvement (skin). Chlorambucil is highly effective, sometimes resulting in dramatic cures. Malignant lymphoproliferative angiitis and granulomatosis corresponds to lymphomatoid granulomatosis. Its lesions show extensive coagulative necrosis, a highly atypical lymphoreticular infiltrate with frequent mitoses, and angioinvasion. Extrapulmonary involvement is frequent (83 per cent), particularly in the skin (46 per cent) and central nervous system (33 per cent). The mortality is high: 65 per cent of the patients were dead within the first year of disease. Although cytotoxic drugs were of no value, corticosteroids were associated with prolonged remissions in three young patients.

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Year:  1977        PMID: 892791     DOI: 10.1016/s0046-8177(77)80004-x

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  12 in total

Review 1.  [Lymphomatoid granulomatosis: differential diagnosis and therapy].

Authors:  M Bohle; K Rasche; K M Müller; G Schultze-Werninghaus; A Fisseler-Eckhoff
Journal:  Med Klin (Munich)       Date:  1999-09-15

Review 2.  Vasculitis and granulomatosis of the respiratory tract.

Authors:  C W Edwards
Journal:  Thorax       Date:  1982-02       Impact factor: 9.139

3.  Lymphomatoid granulomatosis with primary manifestation in the skeletal muscular system.

Authors:  F Schmalzl; R W Gasser; G Weiser; D Zur Nedden
Journal:  Klin Wochenschr       Date:  1982-03

4.  Lymphomatoid granulomatosis: report of a case.

Authors:  C W Edwards; E Nyholm; J Chapman
Journal:  Thorax       Date:  1982-04       Impact factor: 9.139

5.  Wegener's granulomatosis exhibiting the clinical features of Goodpasture's syndrome.

Authors:  G Boros; I Orbán; J Nagy
Journal:  Int Urol Nephrol       Date:  1981       Impact factor: 2.370

6.  Polymorphic reticulosis (lethal midline granuloma) and lymphomatoid granulomatosis: identical or distinct entities?

Authors:  I Stamenkovic; M F Toccanier; Y Kapanci
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1981

7.  Proptosis, hematuria and proteinuria in a 10-year-old girl.

Authors:  R Bortolussi; K Aterman
Journal:  Can Med Assoc J       Date:  1980-06-07       Impact factor: 8.262

8.  Spontaneous pneumothorax in Wegener's granulomatosis.

Authors:  T Jaspan; A M Davison; W C Walker
Journal:  Thorax       Date:  1982-10       Impact factor: 9.139

9.  Mononuclear-cell pulmonary vasculitis in NZB/W mice. I. Histopathologic evaluation of spontaneously occurring pulmonary infiltrates.

Authors:  C Staszak; R J Harbeck
Journal:  Am J Pathol       Date:  1985-07       Impact factor: 4.307

10.  Angiocentric immunoproliferative lesion of the stomach.

Authors:  K Homma; H Umezu; K Nemoto; Y Ohnishi; A Sekine; K Yoshioka
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991
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