Successful embolization and long-term follow-up of a rare neonatal diaphragmatic hemangioma

Wu, Lin; Wang, Ji Mei; Qiao, Z W; Yan, Yongkun; Wang, Lai Shuan

doi:10.1177/2050313x15615471

Cited by 5 publications

(3 citation statements)

References 8 publications

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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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Section: Discussionmentioning

confidence: 99%

Laparoscopic resection of a rare diaphragmatic haemangioma: a case report

et al. 2022

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“…Malignant diaphragmatic tumors include rhabdomyosarcoma, fibrosarcoma, sarcoma, hemangiopericytoma, germ cell tumors, pheochromocytoma, and leiomyosarcoma. Diaphragmatic hemangiomas are extremely rare, and only nine cases have been reported in the English literature to date[2-10] (Table 1).…”

Section: Discussionmentioning

confidence: 99%

“…Most diaphragmatic tumors are benign, including bronchogenic cyst, lipoma, and hemangioma. Diaphragmatic hemangiomas are extremely rare, and only nine cases have been reported in the English literature to date[2-10]. We report a rare case of cavernous hemangioma arising from the diaphragm.…”

Section: Introductionmentioning

confidence: 94%

Three-dimensional image simulation of primary diaphragmatic hemangioma: A case report

Chu

Lin

Kao

et al. 2019

WJCC

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BACKGROUNDFewer than 200 cases of diaphragmatic tumors have been reported in the past century. Diaphragmatic hemangiomas are extremely rare. Only nine cases have been reported in English literature to date. We report a case of cavernous hemangioma arising from the diaphragm. Pre-operative three-dimensional (3D) simulation and minimal invasive thoracoscopic excision were performed successfully, and we describe the radiologic findings and the surgical procedure in the following article.CASE SUMMARYA 40-year-old man was referred for further examination of a mass over the right basal lung without specific symptoms. Contrast-enhanced computed tomography revealed a poorly-enhanced lesion in the right basal lung, abutting to the diaphragm, measuring 3.1 cm × 1.5 cm in size. The mediastinum showed a clear appearance without evidence of abnormal mass or lymphadenopathy. A preoperative 3D image was reconstructed, which revealed a diaphragmatic lesion. Video-assisted thoracic surgery was performed, and a red papillary tumor was found, originating from the right diaphragm. The tumor was resected, and the pathological diagnosis was cavernous hemangioma.CONCLUSIONIn this rare case of diaphragmatic hemangioma, 3D image simulation was helpful for the preoperative evaluation and surgical decision making.

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