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Literature DB >> 14318688

SQUAMOUS CARCINOMA OF THE LUNG WITH OSTEOCARTILAGINOUS STROMA.

Abstract

An instance of a squamous carcinoma of the lung with osteocartilaginous metaplasia in the stroma is reported. This unusual stromal response is similar to extraskeletal osteocartilaginous metaplasia in any other site, and is a change which occasionally is produced by a variety of pathological and experimental conditions, including gastrointestinal adenocarcinoma and urinary tract epithelial carcinoma. This stromal response should be differentiated from a true sarcomatous participation in the tumour.

Entities: Disease

Keywords: CALCINOSIS; CARCINOMA, EPIDERMOID; LUNG NEOPLASMS; NEOPLASM DIAGNOSIS; OSSIFICATION, PATHOLOGIC; PATHOLOGY

Mesh：

Year: 1965 PMID： 14318688 PMCID： PMC472967 DOI： 10.1136/jcp.18.4.403

Source DB: PubMed Journal: J Clin Pathol ISSN： 0021-9746 Impact factor: 3.411

12 in total

Review 3. Pleural chondroid metaplasia in a background of IgG4 plasma cell rich chronic inflammatory infiltrate: report of a rare case with review of literature.

Authors: M Spinelli; A Datta; M A Montero Fenandez; P Viola
Journal: Pathologica Date: 2019-12

3 in total

SQUAMOUS CARCINOMA OF THE LUNG WITH OSTEOCARTILAGINOUS STROMA.

1. Localised myositis ossificans.

2. The stimulation of osteogenesis by urinary bladder tissue.

3. Salivary gland tumours and their mucins.

4. Bony and cartilaginous tumours of the urinary bladder.

5. Osteoid and cartilaginous metaplasia in transplants of rat liver tumours.

6. Two rare breast tumours.

7. Structure and genesis of the mediastinal teratoma.

8. Heterotopic ossification in intestinal neoplasms.

9. A mixed tumour of salivary gland showing bone formation with a histochemical study of the tumour mucoids.

10. Carcinosarcoma of the lung; review of the literature and report of two cases treated by pneumonectomy.

1. Human urinary bladder-carcinoma cells are non-osteoinductive.

2. Pulmonary adenocarcinoma with heterotopic ossification.

Review 3. Pleural chondroid metaplasia in a background of IgG4 plasma cell rich chronic inflammatory infiltrate: report of a rare case with review of literature.