Oriássejtes interstitialis pneumonia.

Translated title of the contribution: Giant cell interstitial pneumonia

P. Barzó, T. Barna, L. Tiszlavicz, A. Kovács

Research output: Contribution to journalReview article

1 Citation (Scopus)

Abstract

GIP is a rarely occurring disorder. There is only few literature from its first description. Authors observed the course of GIP in the case of a 54 year old female patient in the form of bilateral disseminated microfocal pulmonary shadows, increased reticular outline with associated respiratory insufficiency. Open fine needle pulmonary biopsy proved giant cell desquamative alveolitis with help of light- and electronmicroscopical and histochemical examinations. Although possibility of exogenic, inhalative factor or/and infectious origin arose in causing the disease, disposition from the patient's actual immunological status could had helped the evolution of the disease. This fact seemed to be supported by the histologically proven associated dermatitis purpurica pigmentosa (Schamberg disease). With methylprednisolon therapy full radiological recovery occurred, while Schamberg disease was little influenced by the above mentioned therapy. The patient is pulmonologically symptom-free and without complaint after 1 year without any steroid-medication.

Original languageHungarian
Pages (from-to)3079-3083
Number of pages5
JournalOrvosi hetilap
Volume139
Issue number51
Publication statusPublished - Dec 20 1998

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ASJC Scopus subject areas

  • Medicine(all)

Cite this

Barzó, P., Barna, T., Tiszlavicz, L., & Kovács, A. (1998). Oriássejtes interstitialis pneumonia. Orvosi hetilap, 139(51), 3079-3083.