A rare case of lacrimal sac angioleiomyoma managed with dacryocystectomy and turbinectomy

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Standard

A rare case of lacrimal sac angioleiomyoma managed with dacryocystectomy and turbinectomy. / Naeser, Kristian; Pagh, Priyanka; Friis, Per; Heegaard, Steffen.

I: Orbit, Bind 43, Nr. 1, 2024, s. 147-150.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Naeser, K, Pagh, P, Friis, P & Heegaard, S 2024, 'A rare case of lacrimal sac angioleiomyoma managed with dacryocystectomy and turbinectomy', Orbit, bind 43, nr. 1, s. 147-150. https://doi.org/10.1080/01676830.2022.2085306

APA

Naeser, K., Pagh, P., Friis, P., & Heegaard, S. (2024). A rare case of lacrimal sac angioleiomyoma managed with dacryocystectomy and turbinectomy. Orbit, 43(1), 147-150. https://doi.org/10.1080/01676830.2022.2085306

Vancouver

Naeser K, Pagh P, Friis P, Heegaard S. A rare case of lacrimal sac angioleiomyoma managed with dacryocystectomy and turbinectomy. Orbit. 2024;43(1):147-150. https://doi.org/10.1080/01676830.2022.2085306

Author

Naeser, Kristian ; Pagh, Priyanka ; Friis, Per ; Heegaard, Steffen. / A rare case of lacrimal sac angioleiomyoma managed with dacryocystectomy and turbinectomy. I: Orbit. 2024 ; Bind 43, Nr. 1. s. 147-150.

Bibtex

@article{d458f865f95d450a832e9634ea9c9003,
title = "A rare case of lacrimal sac angioleiomyoma managed with dacryocystectomy and turbinectomy",
abstract = "We report a rare case of a lacrimal sac angioleiomyoma. A 56-year-old woman complained of pain in the right medial canthal region over a period of 2 years. There were no complaints of epiphora or ocular infection, and no visible or palpable masses in the medial canthal region. Computed tomography scan revealed a solid tumor of the lacrimal sac expanding to the nasolacrimal duct and protruding under the inferior turbinate. The tumor was removed by external dacryocystectomy combined with endonasal, endoscopic anterior turbinectomy, and nasal mucosal resection. Histological and immunohistological findings were consistent with an angioleiomyoma of the venous type. There was no recurrence of the tumor at the three-year follow-up. Angioleiomyomas should be included in the differential diagnosis of lacrimal sac tumors. The definitive diagnoses rely on histology and immunohistological reactions. The treatment is complete surgical resection.",
keywords = "Angioleiomyoma, dacryocystectomy, lacrimal sac, nasolacrimal duct, turbinectomy, ORBITAL ANGIOLEIOMYOMA, LEIOMYOMA, ANGIOMYOMA",
author = "Kristian Naeser and Priyanka Pagh and Per Friis and Steffen Heegaard",
year = "2024",
doi = "10.1080/01676830.2022.2085306",
language = "English",
volume = "43",
pages = "147--150",
journal = "Orbit",
issn = "0167-6830",
publisher = "Taylor & Francis",
number = "1",

}

RIS

TY - JOUR

T1 - A rare case of lacrimal sac angioleiomyoma managed with dacryocystectomy and turbinectomy

AU - Naeser, Kristian

AU - Pagh, Priyanka

AU - Friis, Per

AU - Heegaard, Steffen

PY - 2024

Y1 - 2024

N2 - We report a rare case of a lacrimal sac angioleiomyoma. A 56-year-old woman complained of pain in the right medial canthal region over a period of 2 years. There were no complaints of epiphora or ocular infection, and no visible or palpable masses in the medial canthal region. Computed tomography scan revealed a solid tumor of the lacrimal sac expanding to the nasolacrimal duct and protruding under the inferior turbinate. The tumor was removed by external dacryocystectomy combined with endonasal, endoscopic anterior turbinectomy, and nasal mucosal resection. Histological and immunohistological findings were consistent with an angioleiomyoma of the venous type. There was no recurrence of the tumor at the three-year follow-up. Angioleiomyomas should be included in the differential diagnosis of lacrimal sac tumors. The definitive diagnoses rely on histology and immunohistological reactions. The treatment is complete surgical resection.

AB - We report a rare case of a lacrimal sac angioleiomyoma. A 56-year-old woman complained of pain in the right medial canthal region over a period of 2 years. There were no complaints of epiphora or ocular infection, and no visible or palpable masses in the medial canthal region. Computed tomography scan revealed a solid tumor of the lacrimal sac expanding to the nasolacrimal duct and protruding under the inferior turbinate. The tumor was removed by external dacryocystectomy combined with endonasal, endoscopic anterior turbinectomy, and nasal mucosal resection. Histological and immunohistological findings were consistent with an angioleiomyoma of the venous type. There was no recurrence of the tumor at the three-year follow-up. Angioleiomyomas should be included in the differential diagnosis of lacrimal sac tumors. The definitive diagnoses rely on histology and immunohistological reactions. The treatment is complete surgical resection.

KW - Angioleiomyoma

KW - dacryocystectomy

KW - lacrimal sac

KW - nasolacrimal duct

KW - turbinectomy

KW - ORBITAL ANGIOLEIOMYOMA

KW - LEIOMYOMA

KW - ANGIOMYOMA

U2 - 10.1080/01676830.2022.2085306

DO - 10.1080/01676830.2022.2085306

M3 - Journal article

C2 - 35678182

VL - 43

SP - 147

EP - 150

JO - Orbit

JF - Orbit

SN - 0167-6830

IS - 1

ER -

ID: 315403316