Cartilage-containing tumours of the lung: Relationship between the purely cartilaginous type (chondroma) and the mixed type (so-called hamartoma): an unusual case of multiple tumours

Bateson, Eric M.

doi:10.1136/thx.22.3.256

Cited by 29 publications

(7 citation statements)

References 17 publications

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“…15). In a previously reported case (Bateson, 1967) there were four chondromas ( fig. ll), three of which consisted entirely of cartilage and connective tissue, but the fourth also contained one epithelium-lined space in the peripheral part of the tumour (fig.…”

Section: Endobronchial Hamartoma and Chondromamentioning

confidence: 85%

Histogenesis of intrapulmonary and endobronchial hamartomas and chondromas (cartilage‐containing tumours): A hypothesis

Bateson

1970

The Journal of Pathology

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Section: Endobronchial Hamartoma and Chondromamentioning

confidence: 85%

Histogenesis of intrapulmonary and endobronchial hamartomas and chondromas (cartilage‐containing tumours): A hypothesis

Bateson

1970

The Journal of Pathology

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“…In the present case it is thought that the aberrant tissue giving rise to the teratoma expanded into the bronchus, instead of the lung parenchyma, which resulted in its endobronchial position. A similar hypothesis has been put forward to explain the difference between pure chondroma and chondromatous hamartoma (mixed tumour) of the lung (Bateson, 1967). BRONCHIECTATIC CHANGES In addition to the bronchiectasis demonstrated bronchographically, which was 'follicular' on pathological examination, there was widespread bronchiolectasis.…”

Section: The Endobronchial Teratomamentioning

confidence: 76%

Endobronchial teratoma associated with bronchiectasis and bronchiolectasis

Bateson¹,

Hayes²,

Woo-Ming³

1968

Thorax

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A teratoma in a young West Indian of Negro race is reported. The teratoma presented radiologically in the left upper lobe as an ill-defined shadow which contained a crescent-shaped translucent area and simulated a mycetoma. In addition, the left lung showed widespread nodular shadows. The left lung was resected and the teratoma was found to be endobronchial in position. This is a very rare site for a teratoma as only one of the 15 previously reported intrapulmonary teratomata may have been endobronchial. The remainder of the left lung remote from the tumour showed generalized bronchiectasis both radiologically and pathologically. The bronchiectasis was of follicular type and in addition there was widespread bronchiolectasis. The inflammatory reaction associated with the latter was responsible for the nodular shadows. The significance of these changes in relation to the teratoma is discussed.

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“…In an earlier series, 100 of 104 soft tissue chondromas arose in the extremities, and only two involved the head and neck [3]. Additional reports have documented soft tissue chondromas in the tongue [9,10], cheek [5], shoulder girdle [5], posterior mediastinum [4], and the lung [6,7,11,12]. Pulmonary chondromas are perhaps best known as a component of the Carney triad [6].…”

Section: Discussionmentioning

confidence: 97%

Soft tissue chondroma of the neck: A case report and review of the literature

González-Crussí

1996

Pediatr Radiol

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We present a case of a soft tissue chondroma arising in the neck of a 5-year-old girl with a 9-month history of respiratory distress and a slowly enlarging right neck mass of uncertain duration. The radiographic, sonographic, and CT features of this lesion will be discussed. This case is unusual due to the relatively rare nature of this lesion, its location, and its occurrence in a young child. This report also emphasizes the need to fully evaluate children with respiratory distress who do not respond to standard medical therapy.

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Cartilage-containing tumours of the lung: Relationship between the purely cartilaginous type (chondroma) and the mixed type (so-called hamartoma): an unusual case of multiple tumours

Cited by 29 publications

References 17 publications

Histogenesis of intrapulmonary and endobronchial hamartomas and chondromas (cartilage‐containing tumours): A hypothesis

Histogenesis of intrapulmonary and endobronchial hamartomas and chondromas (cartilage‐containing tumours): A hypothesis

Endobronchial teratoma associated with bronchiectasis and bronchiolectasis

Soft tissue chondroma of the neck: A case report and review of the literature

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