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Biomedical subjects

H le Brigand

Publications and source records attributed to H le Brigand.

4 recordsLinked to original sources

[71 pulmonary hamarto-chondromas].

Seventy-one hamarto-chondromas were operated on at the Centre Chirurgical Marie-Lannelongue from January the 1st 1958 to September the 1st 1975. Pulmonary hamarto-chondroma is always a slowly evolving benign tumour, usually found in patients between 40 and 60, and twice as frequent in males as in females. There are two different kinds. 1) Intraparenchymal hamarto-chondromas, which have a noteworthy clinical latency and in 2 cases out of 3 are situated anteriorly and peripherally. The usual treatment consists of simple enucleation. 2) Endobronchial hamarto-chondromas, on the other hand, have a striking symptomatology of bronchial obstruction. If operated on after some delay, they will cause the destruction of distal parenchyma. Treatment depends on their topography. Segmental resection is often the sole recourse.

Adolescent↗

[Surgical biopsies of the lung].

Open-chest biopsy performed by an experienced team is a safe way of obtaining samples of suitable size. It is recommended in diffuse pulmonary diseases whose etiology could not be identified by the usual diagnostic means. Pulmonary needle biopsy is a blind method not without risks and should always be performed in the vicinity of a chest surgical unit. Nevertheless it can be considered an initial diagnostic step, followed if unsuccessful by an open-chest biopsy.

Biopsy↗

[Thymoma and lupus disease (apropos of 2 cases].

Two new cases of association between a thymoma and a lupus illness are reported. The first was a women aged 42 years in whom were discovered simultaneously systemic lupus erythematosus (SLE) and a slowly invading thymoma, the histology of which was characterized by the predominance of epithelial cells; excision of this tumour did not appear to affect the evolution of the SLE. In the second case, a patient aged 60 years suffered from SLE ten months after the removal of a benign thymoma in which there was a predominance of lymphocytes. The SLE in this patient was easily controlled for more than a year by small doses of corticoids, but resulted in death after three years when anuria was associated with meningeal signs after the cessation of corticotherapy. The comparision of the data from these cases with those from eleven other cases in which there was association between a thymoma and SLE, brought to light several interesting facts. It is rare that SLE clearly precedes the discovery of the thymoma; it usually occurs afterwards or the two are discovered almost simultaneously. Collagenosis is of importance only when it coexists with a thymoma : starting later much more often than is usual in cases of SLE. The tumours were, in all but two cases, benign thymomas of different histological types, and their removal did not apparently influence the evolution of the SLE.

Adult↗