2008
DOI: 10.1007/s00595-007-3633-2
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Adenocarcinoma arising in anterior mediastinal mature cystic teratoma: Report of a case

Abstract: Mediastinal mature teratoma with malignant components is a very rare condition. A 57-year-old man presented with a large (14 x 10 cm) encapsulated and lobulated cystic mass involving the anterior mediastinum. The most consistent diagnosis on the basis of radiological findings was mature cystic teratoma, and a surgical resection was thus indicated. The operation was performed through a median sternotomy, and the tumor was extirpated with a combined resection of the pericardium and left mediastinal pleura. Altho… Show more

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Cited by 22 publications
(19 citation statements)
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“…A minimum size of one low-power field has been suggested as the threshold for the diagnosis of somatic-type malignancy in germ cell tumors [1,2]. The majority of reports of somatictype malignancy in teratomas has described a single histological type of malignancy [4,7]. However, Armah et al [8] described a renal teratoma similar to our case, where coexisting adenocarcinoma and carcinoid tumor were seen.…”
Section: Discussioncontrasting
confidence: 48%
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“…A minimum size of one low-power field has been suggested as the threshold for the diagnosis of somatic-type malignancy in germ cell tumors [1,2]. The majority of reports of somatictype malignancy in teratomas has described a single histological type of malignancy [4,7]. However, Armah et al [8] described a renal teratoma similar to our case, where coexisting adenocarcinoma and carcinoid tumor were seen.…”
Section: Discussioncontrasting
confidence: 48%
“…It accounts for 5%-10% of all mediastinal tumors [1]. The coexistence of a malignant component in mature teratoma is extremely rare [1,4,6]. Non-germ cell malignancies arising in a teratoma have been described as teratoma with malignant transformation [1,2,4].…”
Section: Discussionmentioning
confidence: 99%
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“…Only one case was from primary mediastinal tumour and mediastinal lymphoma respectively 5 . Primary adenocarcinoma of mediastinum is very rare although it has been sporadically reported for example a originating from a calcified nodule or mature teratoma 6,7 . More commonly, the lesion is a secondary metastasis from lung, gastrointestinal tract, pancreas, kidney or even the pituitary gland 3 .…”
Section: Discussionmentioning
confidence: 99%