Cellular angiofibroma of the vulva: case report with clinicopathological and immunohistochemistry study

CONTEXT: Cellular angiofibroma of the vulva is a rare tumor that was first described in 1997. It occurs in middle-aged women (average age: 47 years), has small size (< 3 cm) and well-circumscribed margins. CASE REPORT: We describe a case in a 51-year-old woman whose preoperative diagnosis was confounded with Bartholin's glandular cyst. The neoplasia was well delimited and made up of three characteristic components: fusiform cells forming small fascicles, numerous blood vessels and adipose tissue interspersed between the fusiform cells. The stroma cells were positive for vimentin and negative for CD34, protein S-100, actin and desmin. The differential diagnoses for this tumor include aggressive angiomyxoma, angiomyofibroblastoma, lipoma of fusiform cells, solitary fibrous tumor, perineurioma and leiomyoma.

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Aggressive Angiomyxoma Pelvis Presenting as an Ovarian Tumor with Vault Prolapse

Journal of Postgraduate Medicine Education and Research ◽

10.5005/jp-journals-10028-1022 ◽

2012 ◽

Vol 46 (2) ◽

pp. 102-103

Author(s):

Lakhbir Dhaliwal ◽

Neelam Aggarwal ◽

Raje Nijhawan ◽

Subhas Chandra Saha

Keyword(s):

Case Report ◽

Ovarian Tumor ◽

Preoperative Diagnosis ◽

Rare Case ◽

Diagnosis And Treatment ◽

Aggressive Angiomyxoma ◽

Rare Tumor ◽

Pelvic Tumor ◽

Vault Prolapse

ABSTRACT Background Angiomyxoma is a rare tumor arising from the pelvis. Preoperative diagnosis and treatment may be difficult. Case report We report a rare case of aggressive angiomyxoma pelvis that presented as vault prolapse and was misdiagnosed as ovarian tumor. Conclusion As surgery is the main treatment, preoperative diagnosis and assessment of extent of the tumor for planning surgery cannot be overemphasized. Synopsis Angiomyxoma is a rare pelvic tumor with varied presentation. Preoperative diagnosis and assessment of extent of the tumor are important for its management. How to cite this article Siwatch S, Saha SC, Aggarwal N, Dhaliwal L, Nijhawan R. Aggressive Angiomyxoma Pelvis Presenting as an Ovarian Tumor with Vault Prolapse. J Postgrad Med Edu Res 2012;46(2):102-103.

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Preoperative diagnosis of solitary fibrous tumor of the kidney with percutaneous fine needle biopsy and management with laparoscopic partial nephrectomy: One case report and literatures review

Chinese Journal of Clinical Oncology ◽

10.1007/s11805-008-0453-0 ◽

2008 ◽

Vol 5 (6) ◽

pp. 453-455 ◽

Cited By ~ 1

Author(s):

Liaoyuan Li ◽

Yadi He ◽

Xin Gao ◽

Ming Yang ◽

Haibin Zhang ◽

...

Keyword(s):

Case Report ◽

Partial Nephrectomy ◽

Solitary Fibrous Tumor ◽

Needle Biopsy ◽

Preoperative Diagnosis ◽

Fine Needle Biopsy ◽

Laparoscopic Partial Nephrectomy ◽

Fine Needle ◽

Fibrous Tumor

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Solitary fibrous tumor, a rare tumor of the pleura: A case report

Respiratory Medicine CME ◽

10.1016/j.rmedc.2008.10.009 ◽

2009 ◽

Vol 2 (2) ◽

pp. 84-85 ◽

Cited By ~ 1

Author(s):

L.J. van Eijsden ◽

G.J.M. Akkersdijk ◽

K. van Groningen ◽

C.F. Melissant

Keyword(s):

Case Report ◽

Solitary Fibrous Tumor ◽

Rare Tumor ◽

Fibrous Tumor

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Intravascular large B-cell lymphoma involving pleural solitary fibrous tumor: A case report and literature review

Human Pathology Case Reports ◽

10.1016/j.ehpc.2021.200530 ◽

2021 ◽

Vol 25 ◽

pp. 200530

Author(s):

Amintas Samuel ◽

Laurent Elodie ◽

Gros Audrey ◽

Sesboue Come ◽

Merlio Jean-Philippe ◽

...

Keyword(s):

Case Report ◽

Literature Review ◽

B Cell ◽

Solitary Fibrous Tumor ◽

Cell Lymphoma ◽

B Cell Lymphoma ◽

Large B Cell Lymphoma ◽

Fibrous Tumor ◽

Large B Cell

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Retroperitoneal fibrous tumor recurring as lung metastases after 10 years: a case report

Surgical Case Reports ◽

10.1186/s40792-021-01209-4 ◽

2021 ◽

Vol 7 (1) ◽

Author(s):

Kozue Matsuishi ◽

Kojiro Eto ◽

Atsushi Morito ◽

Hirokazu Hamasaki ◽

Keisuke Morita ◽

...

Keyword(s):

Case Report ◽

Solitary Fibrous Tumor ◽

Distant Metastasis ◽

Curative Resection ◽

Lung Metastases ◽

Lung Resection ◽

Left Lung ◽

Metastatic Lesion ◽

Case Presentation ◽

Fibrous Tumor

Abstract Background Solitary fibrous tumor (SFT) is a relatively rare mesenchymal tumor that mainly affects adults. Its prognosis is good after curative resection, but distant recurrences after 10 years or longer have been reported. Recurrent SFT usually arises as a local lesion; distant metastasis is rarely reported. Here, we report lung metastases that recurred a decade after excising a retroperitoneal primary SFT. Case presentation A 44-year-old woman had an SFT resected from her right retroperitoneum at our hospital. Ten years later, at age 54, she underwent a lung resection after CT showed three suspected metastases in her left lung. All three were histologically diagnosed as lung metastases from the retroperitoneal SFT. However, whereas the primary SFT had 1–2 mitotic cells/10 high power fields (HPF), the metastatic lesion increased malignancy, at 50/10 HPF. Conclusion Patients who have had resected SFTs should be carefully followed up, as malignancy may change in distant metastasis, as in this case.

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