Cavernous hemangioma arising from the diaphragm

Ueno, Kensuke; Takeuchi, Eriho; Hino, Haruaki; Kawashima, M

doi:10.1177/0218492312469361

Cited by 5 publications

(2 citation statements)

References 7 publications

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“…According to this, a complete resection should be recommended. 33,34 Furthermore, other benign diaphragmatic tumors have been reported such as chondroma, 35 schwannoma, 6 haemangioma, 7 neurofibroma, angiofibroma, endothelioma, leiomyoma, or rhabdomyofibroma. 8 The removal of these tumors allows the histologic examination and achieves a good prognosis.…”

Section: Primary Diaphragmatic Tumors Primary Benign Tumors Of the DImentioning

confidence: 99%

Primary and Secondary Tumors of the Diaphragm

Baldes

Schirren

2016

Thorac cardiovasc Surg

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Section: Primary Diaphragmatic Tumors Primary Benign Tumors Of the DImentioning

confidence: 99%

Primary and Secondary Tumors of the Diaphragm

Baldes

Schirren

2016

Thorac cardiovasc Surg

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“…6 A search of the PubMed V R database identified 10 case reports on diaphragmatic haemangiomas published in English. 3,[6][7][8][9][10][11][12][13][14][15] A definitive preoperative diagnosis of diaphragmatic haemangioma is difficult to obtain on imaging due to its physiological characteristics. A similar situation exists with other haemangiomas.…”

Section: Discussionmentioning

confidence: 99%

Laparoscopic resection of a rare diaphragmatic haemangioma: a case report

et al. 2022

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This case report describes the laparoscopic resection of a rare diaphragmatic haemangioma. A 45-year-old male patient was diagnosed incidentally with a left subphrenic mass by computed tomography. Laparoscopic left subphrenic mass excision was performed under general anaesthesia. A phrenic haemangioma was confirmed by postoperative pathology. Tumours originating in the diaphragm are rare, with only approximately 200 cases reported in the past century. The diaphragmatic tumour was determined to be primary because intraoperative imaging showed that the tumour was relatively isolated and had no obvious relationship with the surrounding tissues and organs.

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A case of diaphragmatic hemangioma completely resected by partial diaphragmatic resection

Mori

Nose

Hamahiro

et al. 2022

Journal of Surgical Case Reports

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Diaphragmatic hemangiomas are rare tumors and the preferred resection range in surgical procedures is considered on a case-by-case basis. We report a case of diaphragmatic hemangioma that was completely resected by partial diaphragmatic resection. An 81-year-old man was referred for the examination of right diaphragmatic mass. Computed tomography revealed two contrast-enhanced nodules (diameter: 17 and 10 mm, respectively) on the right diaphragm. The nodules were completely resected by partial resection of the diaphragm via video-assisted thoracic surgery using an ultrasonic coagulation and incision device. Resection was performed leaving part of the muscular layer of the diaphragm. Histopathology confirmed the nodule to be hemangioma originating from the diaphragm and no hemangiomatous lesions were noted in the normal connective tissue in the resected stump. Partial diaphragmatic resection is a less invasive treatment method and may be a useful surgical procedure for diaphragmatic hemangioma.

show abstract

Cavernous hemangioma arising from the diaphragm

Cited by 5 publications

References 7 publications

Primary and Secondary Tumors of the Diaphragm

Primary and Secondary Tumors of the Diaphragm

Laparoscopic resection of a rare diaphragmatic haemangioma: a case report

A case of diaphragmatic hemangioma completely resected by partial diaphragmatic resection

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