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Journal articles on the topic 'Broad ligament tumor'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Sultana, Nahid, Masuma Jalil, Fateha Ferdous, Shahnaz Rahman, and Rahima Begum. "Broad Ligament Fibroid: A Diagnostic Dilemma." BIRDEM Medical Journal 5, no. 2 (2016): 116–18. http://dx.doi.org/10.3329/birdem.v5i2.28392.

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Leiomyomas are the commonest of all pelvic tumors. One-fifth women of reproductive age group suffer from this condition. Tumors of broad ligament are rare. Most common solid tumor of the broad ligament is a leiomyoma. It can originate from the uterus or broad ligament itself. Here, we report a case of broad ligament leiomyoma in a woman having secondary infertility and it posed a diagnostic dilemma.Birdem Med J 2015; 5(2): 116-118

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2

Kuo, Kuan-Ting, Mei-Jou Chen, and Ming-Chieh Lin. "Epithelioid Trophoblastic Tumor of the Broad Ligament." American Journal of Surgical Pathology 28, no. 3 (2004): 405–9. http://dx.doi.org/10.1097/00000478-200403000-00017.

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3

Czernobilsky, Bernard, Beatriz Lifschitz-Mercer, Leonor Trejo, and Ilan Atlas. "Granulosa Cell Tumor of the Broad Ligament." International Journal of Surgical Pathology 19, no. 6 (2009): 783–86. http://dx.doi.org/10.1177/1066896909356104.

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4

Jafri, Nayyer H., Theodore H. Niemann, James L. Nicklin, and Larry J. Copeland. "A CARCINOID TUMOR OF THE BROAD LIGAMENT." Obstetrics & Gynecology 92, Supplement (1998): 708. http://dx.doi.org/10.1097/00006250-199810001-00031.

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5

JAFRI, N. "A carcinoid tumor of the broad ligament." Obstetrics & Gynecology 92, no. 4 (1998): 708. http://dx.doi.org/10.1016/s0029-7844(98)00174-4.

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6

Malik, Roopa, Krishna Dahiya, Isha Nandal, and Alisha Goyal. "Broad Ligament Leiomyoma Masquerading as Ovarian Tumor." Journal of South Asian Federation of Obstetrics and Gynaecology 15, no. 2 (2023): 251–53. http://dx.doi.org/10.5005/jp-journals-10006-2140.

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7

Mallick, D., M. Saha, S. Chakrabarti, and J. Chakraborty. "Leiomyoma of Broad Ligament Mimicking Ovarian Malignancy– Report of a Unique Case." Kathmandu University Medical Journal 12, no. 3 (2015): 219–21. http://dx.doi.org/10.3126/kumj.v12i3.13723.

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Tumors of the broad ligament are uncommon. Leiomyoma, which is the commonest female genital neoplasm, is also the most common solid tumor of the broad ligament. Leiomyomas affect 30% of all women of reproductive age but the incidence of broad-ligament leiomyoma is <1%. These benign tumors are usually asymptomatic. A case is being described where a 52 year old presented with gradual abdominal swelling which was clinically and radiologically diagnosed as ovarian malignancy. On abdominal and bimanual palpation a soft cystic mass was noted in the right pelvic region. CA 125 was mildly raised. C

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8

Singh, Lata, Taru Gupta, Snigdha Kumari, and Sangeeta Gupta. "True broad ligament fibroid mimicking ovarian mass in a postmenopausal woman." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 8, no. 7 (2019): 2910. http://dx.doi.org/10.18203/2320-1770.ijrcog20193067.

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Fibroids are benign smooth muscle tumors. Large fibroids are known to arise from the uterus, but occasionally from the broad ligament. Here, we report a case of true broad ligament fibroid which is rare and difficult to diagnose in a 57 year old postmenopausal women with a large mass of 24 weeks size gravid uterus. Patient presented with pain lower abdomen and mass in abdomen with no other co-morbidity. This broad ligament fibroid was mimicking as ovarian tumor on ultrasonography and MRI as left ovary was not visualised separately, thus leading to diagnostic dilemma of ovarian malignancy. Mass

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9

Manogna, L., and Kavitha a. "BROAD LIGAMENT FIBROID MIMICKING AS OVARIAN FIBROMA." International Journal of Advanced Research 11, no. 01 (2023): 762–64. http://dx.doi.org/10.21474/ijar01/16077.

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Fibroid uterus is the most common benign tumor of uterus. Extrauterine fibroids are rare and most common extra uterine fibroid is broad ligament fibroid. Broad ligament fibroids are difficult to diagnose and treat. Most often misdiagnosed as ovarian malignancy. In our case ovarian fibroma was suspected and ultrasound pelvis,CT and MRI reports suggestive of ovarian fibroma. Intraoperative findings suggestive of Broad ligament fibroid, fibroid excision was done along with abdominal total hysterectomy and bilateral salpingoo oophorectomy. Diagnosis was confirmed by intraoperative findings and his

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10

Oliveira, João Diogo, Teresa Margarida Cunha, and Andreia Tereso. "Tumors of the broad ligament: what and when to suspect such rare location." Radiologia Brasileira 53, no. 5 (2020): 349–55. http://dx.doi.org/10.1590/0100-3984.2019.0073.

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Abstract Although secondary involvement of the broad ligament by malignant tumors arising elsewhere in the abdomen and pelvis is common, primary tumors in this location are rare. Tumors of the broad ligament can be of mesenchymal and mixed nature, such as leiomyoma, the most common neoplasm; epithelial tumors of Müllerian type, imposing a challenge to differentiate them from other adnexal masses; unique tumors from mesonephric origin; and tumor-like lesions. Most neoplasms in this region, whether benign or malignant, usually present clinically with vague symptoms and are often discovered durin

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11

Sadovsky, P. "34. Gross. Contribution à l’étude des fibromyomes du ligament large (Sixième Congrès de Français de Chirurgie. Semaine Medicale № 19). To scholarship on fibromyomas of the broad ligament." Journal of obstetrics and women's diseases 7, no. 2 (2020): 192. http://dx.doi.org/10.17816/jowd72192.

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Dense tumors of the broad ligament are extremely rare and poorly understood. Virchow was the first to point out the possibility of direct development of fibroids from the tissues of the broad ligament. Schetelig, Langenbeck, Gayet, Billroth, Schroeder, Tedenert, et al. Observed intraligamentary fibroids without a connection to the uterus. Fibromyomas on the stem are much more demonstrative, but they come across even more often; so far only 5 cases have been published: Mikulicz, Snger, Borker, Biflinger and Doran. The author removed the pedicle fibromyoma with a total of 2500 grams from the rig

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12

Whittemore, Darren E., Robert E. Grondahl, and Kondi Wong. "Primary Extraneural Myxopapillary Ependymoma of the Broad Ligament." Archives of Pathology & Laboratory Medicine 129, no. 10 (2005): 1338–42. http://dx.doi.org/10.5858/2005-129-1338-pemeot.

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Abstract Primary extraneural ependymomas are rare tumors that arise in ectopic sites, including pulmonary, sacrococcygeal region, ovarian, and paraovarian tissues. Four such ependymomas reported in the literature involve the paraovarian tissues, including 2 broad ligament ependymomas. Here we describe a myxopapillary ependymoma of the broad ligament in a 22-year-old woman, which may be the first tumor of this type to be reported in this location. Cytology, histology, cytochemistry, immunohistochemistry, and flow cytometry ploidy analysis are studied and described. Identification of perivascula

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13

Jagtap, Sunil Vitthalrao, Nitesh Nasre, Nitin S. Kshirsagar, and Shubham S. Jagtap. "Aggressive angiomyxoma of broad ligament: an uncommon mesenchymal tumor." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 8, no. 7 (2019): 2913. http://dx.doi.org/10.18203/2320-1770.ijrcog20193068.

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Aggressive angiomyxoma is a rare mesenchymal tumor occurring predominantly in the pelviperineal region. Authors present a case of a 70 years female presented with history of distention of lower abdomen with recurrent pain since 6 months. On clinical examination there was suspicion of fibroid. On USG it was reported as huge fleshy, soft tissue mass measuring 20x10x9 cm in lower abdominal flanks and pelvis with vascular pedicle attached to right parametrium. Pan-hysterectomy was performed. Right broad ligament showed mass measuring 18.5x10x6 cm. On histopathological examination it was diagnosed

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14

MURIALDO, R., A. USSET, T. GUIDO, F. CARLI, F. BOCCARDO, and D. AMOROSO. "Leiomyosarcoma of the broad ligament: a case report and review of literature." International Journal of Gynecologic Cancer 15, no. 6 (2005): 1226–29. http://dx.doi.org/10.1136/ijgc-00009577-200511000-00046.

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Leiomyosarcoma of the broad ligament is a rare tumor, since only 12 cases have been reported so far in the literature. A 53-year-old patient was diagnosed with leiomyosarcoma of the broad ligament at the Department of Gynecology Oncology of the National Cancer Research Institute in Genoa. The tumor had low mitotic activity and less than ten mitotic figures were found for ten high-power fields. The treatment consisted of total abdominal hysterectomy and bilateral salpingo-oophorectomy with bilateral ureteral neoanastomosis and omentectomy. The patient has not received either radiotherapy or che

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15

Kumari, Rajesh, Vandana Vaishya, Vidushi Kulshrestha, Jai Bhagwan Sharma, and Alka Kriplani. "A case of broad ligament leiomyoma presenting as an ovarian mass." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 6, no. 6 (2017): 2635. http://dx.doi.org/10.18203/2320-1770.ijrcog20172369.

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The broad ligament is the commonest extra uterine site for the occurrence of leiomyoma but with a very low incidence rate. It poses both clinical and radiological challenge in differentiating from an ovarian tumour. A 25-year-old unmarried female presented with history of lower abdominal pain associated with rapidly increasing abdominal distension for last 3 months. General physical examination was unremarkable. Examination of the abdomen revealed a firm, non-tender mass, with limited mobility arising from the pelvis corresponding to a uterine size of 32 weeks. Ultrasonography of abdomen revea

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16

Mauricio, D. D., and G. Vanderlee. "High grade unclassified sarcoma of the broad ligament: A case report and literature review." Journal of Clinical Oncology 25, no. 18_suppl (2007): 20536. http://dx.doi.org/10.1200/jco.2007.25.18_suppl.20536.

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20536 Background: The incidence of primary sarcoma of the broad ligament is very rare. From the first reported finding in 1968, there are only 17 documented cases worldwide of this very progressive and highly malignant gynecologic neoplasm. We present the 18th case of this aggressive tumor to add to the scarce knowledge about this disease and to contribute in characterizing its behavior and its reasonable management. Methods: Case report and case review/series Results: This is the 18th case of broad ligament sarcoma found on routine physical examination in a woman who had previous hysterectomy

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17

Sassi, Farah, Ghada Sahraoui, Lamia Charfi, Zemni Ines, Karima Mrad, and Raoudha Doghri. "A rare case report of a myxoid liposarcoma arising from the broad ligament." Rare Tumors 14 (January 2022): 203636132211488. http://dx.doi.org/10.1177/20363613221148839.

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Myxoid liposarcoma (MLPS) is the second most prevalent subtype of liposarcoma. It is usually found in the deep tissues of the lower limbs and rarely in gynecologic tract. Herein we present the second case in the English literature of a primary MLPS arising from the broad ligament which was thought to be a borderline ovarian tumor. The aim is to discuss its clinical and pathological characteristics. A 42-year-old woman presented with pelvic pain for the last 6 months. Magnetic resonance imaging was not specific. She underwent a surgical resection of the tumor mass, and pathological examination

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18

Chen, Sijing, Ying Zheng, Lin Chen, and Qihua Yi. "A broad ligament solitary fibrous tumor with Doege–Potter syndrome." Medicine 97, no. 39 (2018): e12564. http://dx.doi.org/10.1097/md.0000000000012564.

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19

Itani, Y., K. Itoh, S. Adachi, et al. "Malignant epithelial tumor of unknown origin of the broad ligament." Archives of Gynecology and Obstetrics 267, no. 2 (2002): 113–16. http://dx.doi.org/10.1007/s00404-001-0264-5.

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20

Mrad, Karima, Maha Driss, Salma Abdelmoula, Samia Sassi, Monia Hechiche, and Khaled Ben Romdhane. "Primary Broad Ligament Cystadenocarcinoma With Mucinous Component: A Case Report With Immunohistochemical Study." Archives of Pathology & Laboratory Medicine 129, no. 2 (2005): 244–46. http://dx.doi.org/10.5858/2005-129-244-pblcwm.

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Abstract Primary cystadenocarcinoma that arises in the broad ligament is extremely rare, especially when it is mucinous. We report the case of a 59-year-old woman with a cystic mass of the right broad ligament who underwent a complete excision of the mass (7 × 7 × 3 cm) with hysterectomy, right salpingo-oophorectomy, omentectomy, appendicectomy, and peritoneal biopsies. Pathologic examination showed a low-grade cystadenocarcinoma with a mucinous component limited to the broad ligament. Despite the chemotherapy (cisplatinum and cyclophosphamide) performed, early tumor recurrence occurred after

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21

Liu, Siman, Xiu Lin, Yujie Huang, and Zhong Lin. "Laparoscopic surgery for broad ligament adenomyoma: A case report and literature review." Medicine 104, no. 28 (2025): e43399. https://doi.org/10.1097/md.0000000000043399.

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Rationale: Adenomyoma of the broad ligament is rare. Owing to the absence of typical clinical signs and imaging methods, preoperative diagnosis is challenging, and it is mainly diagnosed through surgical pathology. Patient concerns: The patient experienced recurrent lower abdominal pain for 4 years. Treatments with traditional Chinese medicine and anti-inflammatory drugs were ineffective, and painkillers became less effective over time owing to resistance. Multiple ultrasounds revealed a mass in the right adnexa, but gynecological tumor markers were normal. Diagnosis: The preoperative diagnosi

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22

Fink, D., D. E. Marsden, L. Edwards, C. Camaris, and N. F. Hacker. "Malignant perivascular epithelioid cell tumor (PEComa) arising in the broad ligament." International Journal of Gynecologic Cancer 14, no. 5 (2004): 1036–39. http://dx.doi.org/10.1136/ijgc-00009577-200409000-00045.

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Malignant perivascular epithelioid cell tumor (PEComa) is an extremely rare mesenchymal neoplasm mostly composed of HMB-45-positive epithelioid cells with clear-to-eosinophilic cytoplasm, a propensity for perivascular distribution and a coexpression of smooth muscle markers. The uterus seems to be one of the most prevalent sites of involvement, although only 14 cases of uterine PEComa have been described. We report the case of a 51-year-old woman with a PEComa arising in the broad ligament. She was treated with total abdominal hysterectomy, bilateral salpingo-oophorectomy, omentectomy, and pel

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23

Rajanna, Dayananda Kumar, Vaibhav Pandey, Sujit Janardhan, and Sujatha N. Datti. "Broad Ligament Fibroid Mimicking as Ovarian Tumor on Ultrasonography and Computed Tomography Scan." Journal of Clinical Imaging Science 3 (February 28, 2013): 8. http://dx.doi.org/10.4103/2156-7514.107912.

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Giant fibroids are known to arise from the uterus, and very rarely from the broad ligament. Large fibroids often undergo hyaline, cystic, and at times, red degeneration. In the present case, cystic degeneration with intervening septations in an adnexal mass raised the suspicion of ovarian neoplasm as the ovaries were not seen as separate from the lesion. The ultrasonographic and contrast-enhanced computed tomographic findings of this case were characteristic of ovarian neoplasm. The differential diagnosis included rare possibility of giant fibroid with cystic degeneration. The diagnosis was co

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24

Kim, Hae Kyung, Ju Hyun Kim, Sung Yeon Hong, Youn Seok Choi, Hoon Kyu Oh, and Tae Sung Lee. "A uterine lipoleiomyoma of the broad ligament mimicking an ovarian tumor." Korean Journal of Obstetrics & Gynecology 55, no. 10 (2012): 787. http://dx.doi.org/10.5468/kjog.2012.55.10.787.

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25

Itoga, Tomoko, Toshiharu Matsumoto, Chikako Suzuki, et al. "Peritoneal endometriosis in the broad ligament presenting as a large tumor." Pathology International 52, no. 5-6 (2002): 410–15. http://dx.doi.org/10.1046/j.1440-1827.2002.01363.x.

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26

Inukai, Ryo, Tatsuya Kawai, Ryutaro Nishikawa, et al. "Ependymoma of the broad ligament mimicking an ovarian surface epithelial tumor." Radiology Case Reports 16, no. 1 (2021): 210–14. http://dx.doi.org/10.1016/j.radcr.2020.10.046.

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27

Fink, D., D. E. Marsden, L. Edwards, C. Camaris, and N. F. Hacker. "Malignant perivascular epithelioid cell tumor (PEComa) arising in the broad ligament." International Journal of Gynecological Cancer 14, no. 5 (2004): 1036–39. http://dx.doi.org/10.1111/j.1048-891x.2004.014549.x.

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28

Kim, Hyun-Jung, Sung-Jig Lim, Hoon Choi, and Kyeongmee Park. "Malignant clear-cell myomelanocytic tumor of broad ligament—a case report." Virchows Archiv 448, no. 6 (2006): 867–70. http://dx.doi.org/10.1007/s00428-006-0161-1.

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29

Fras, Albert Peter, and Snježana Frković-Grazio. "Hyalinizing Spindle Cell Tumor with Giant Rosettes of the Broad Ligament." Gynecologic Oncology 83, no. 2 (2001): 405–8. http://dx.doi.org/10.1006/gyno.2001.6368.

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30

Zubor, Pavol, Karol Kajo, Norbert Szunyogh, Silvester Galo, and Jan Danko. "A solitary fibrous tumor in the broad ligament of the uterus." Pathology - Research and Practice 203, no. 7 (2007): 555–60. http://dx.doi.org/10.1016/j.prp.2007.02.005.

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31

Itonaga, Yui, Masakazu Nishida, Harunobu Matsumoto, Kaei Nasu, and Hisashi Narahara. "A Case of Neuroendocrine Carcinoma Developing from the Broad Ligament of the Uterus." Rare Tumors 9, no. 2 (2017): 57–59. http://dx.doi.org/10.4081/rt.2017.6958.

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Neuroendocrine carcinoma (NEC), also called small cell carcinoma or large cell carcinoma, is a rare and aggressive tumor that develops mainly in the lung and intestine. More rarely, NEC develops in gynecologic organs, with poor prognoses. We experienced a case of NEC in the broad ligament of the uterus. The patient was a 74-year-old woman with symptoms of abdominal distension and constipation. Ultrasound sonography detected an abdominal tumor larger than 10 cm. She was then admitted to our hospital. She underwent surgery under the diagnosis of ovarian cancer, but the bilateral ovaries and uter

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32

Basnyat, Amogh, Ganesh Dangal, Aruna Karki, Hema Pradhan, Ranjana Shrestha, and Kabin Bhattachan. "Broad Ligament Leiomyomata - An Important Differential Diagnosis in Huge Abdominal Mass: A Case Report." Journal of Nepal Medical Association 63, no. 283 (2025): 186–88. https://doi.org/10.31729/jnma.8908.

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Leiomyomas are a common gynaecological condition affecting 20-30% of women over the age of 35, with prevalence decreasing following menopause. Leiomyomas are most commonly found within the uterus. Rarer extra-uterine locations include the broad ligament, cervix, and vagina. We present an unusual case of multiple Left Broad Ligament Leiomyomata that extended from Left Iliac Fossa and Hypogastrium to Epigastric region in a 50- year-old female. Our case highlights the importance for extra-uterine leiomyoma to be considered as a differential diagnosis in patients presenting with huge abdominal mas

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33

Barcia, Sara M., Alp Usubutun, and Joseph T. Rabban. "Immunophenotypic Similarity of Papillary Cystadenoma of the Broad Ligament and Mesonephric Remnants of Broad Ligament: Implications for Tumor Origin and Differential Diagnosis." American Journal of Clinical Pathology 138, suppl 2 (2012): A288. http://dx.doi.org/10.1093/ajcp/138.suppl2.239.

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34

Mulvany, Nick J. N. "Atlas of Tumor Pathology: Tumors of the Ovary, Maldeveloped Gonads, Fallopian Tube, and Broad Ligament." Pathology 32, no. 1 (2000): 65. http://dx.doi.org/10.1016/s0031-3025(16)34729-8.

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35

Mandade, Krishna, Kashika Singh, Aptulkar, Angarkar, and DP Bhavthankar. "Aggressive angiomyxoma presenting as huge broad ligament tumor-A rare case report." International Journal of Medical Research & Health Sciences 3, no. 1 (2014): 186. http://dx.doi.org/10.5958/j.2319-5886.3.1.038.

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36

Coggeshall, Jason D., Joanne N. Franks, Diane U. Wilson, and Jennifer L. Wiley. "Primary Ovarian Teratoma and GCT with Intra-abdominal Metastasis in a Dog." Journal of the American Animal Hospital Association 48, no. 6 (2012): 424–28. http://dx.doi.org/10.5326/jaaha-ms-5809.

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This report describes the simultaneous occurrence of an ovarian teratoma and a granulosa cell tumor (GCT) with intra-abdominal metastasis in a 1.5 yr old female Doberman pinscher. At surgery, a 20 cm, smooth, intact mass associated with the left ovary and multiple 1–2 cm irregular masses in the broad ligament were found. The masses were surgically removed and submitted for histopathology. A histologic diagnosis of a teratoma and a GCT with broad ligament metastasis was made. Further treatment was elected by the owner and included two cycles of carboplatin therapy. The dog was euthanized 6 wk p

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37

Mir, Ruquaya, VP Singh, Sushma Sinha, and Deepshikha Arora. "Unusual Broad Ligament Tumor - Ancient Schwannoma: A Case Report and Review of Literature." Apollo Medicine 6, no. 3 (2009): 209–11. http://dx.doi.org/10.1177/0976001620090303.

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38

Mir, Ruquaya, VP Singh, Sushma Sinha, and Deepshikha Arora. "Unusual Broad Ligament Tumor - Ancient Schwannoma: A Case Report and Review of Literature." Apollo Medicine 6, no. 3 (2009): 209–11. http://dx.doi.org/10.1016/s0976-0016(11)60529-2.

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39

Utnal, Preeti, Supreetha MS, and Sheela S R. "Serous Cystadenocarcinoma with Fibroma of left ovary and epithelial dysplasia of left fallopian tube - A Case report." JOURNAL OF CLINICAL AND BIOMEDICAL SCIENCES 10, no. 1 (2020): 37–40. http://dx.doi.org/10.58739/jcbs/v10i1.3.

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Collision tumors are best considered as separate primary neoplasms. These tumors have been reported in various organs, such as the esophagus, stomach, liver, thyroid gland, ovary, and lung, but they are extremely rare in the ovaries. Here we report a case of rare collision tumor of Serous cystadenocarcinoma with Fibroma of ovary and Dysplasia of fallopian tube in a 75 year old female who presented with history of pain abdomen and postmenopausal bleeding and was clinically and radiologically diagnosed as Broad ligament fibroid. Keywords: Ovary , serous cystadenocarcinoma, fibroma

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40

Sheyn, Irena, Jose L. Mira, Pablo A. Bejarano, and Nader Husseinzadeh. "Metastatic Female Adnexal Tumor of Probable Wolffian Origin." Archives of Pathology & Laboratory Medicine 124, no. 3 (2000): 431–34. http://dx.doi.org/10.5858/2000-124-0431-mfatop.

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Abstract Female adnexal tumor of probable wolffian origin is a rare neoplasm that can present diagnostic difficulties. We report herein a case of a 60-year-old woman with female adnexal tumor of probable wolffian origin arising within the leaves of a broad ligament and, 5 years later, presenting with metastasis to the liver. The morphologic, immunohistochemical, ultrastructural, and DNA ploidy findings of the original and metastatic tumor, differential diagnoses, and the results of the English-language literature review are presented.

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41

Kakushkin, N. "Female doctor M. Volkova. A case of treatment of non-operated uterine fibroids by means of vibrations. (Proceedings of the General Russian doctors in St. Petersburg for 1893-1894, March)." Journal of obstetrics and women's diseases 8, no. 10 (2020): 933. http://dx.doi.org/10.17816/jowd810933.

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Married, nulliparous, 35 years old, fell ill after severe traumatic injury. Nearby with a retroperitoneal tumor (partly interconnective in the direction of the left broad ligament), there was a whole series of common nervous disorders that went parallel with the decline in nutrition and exhaustion due to blood loss.

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42

GURBUZ, A., A. KARATEKE, C. KABACA, H. ARIK, and R. BILGIC. "A case of cotyledonoid leiomyoma and review of the literature." International Journal of Gynecologic Cancer 15, no. 6 (2005): 1218–21. http://dx.doi.org/10.1136/ijgc-00009577-200511000-00044.

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We report a case of a rare, unusual benign tumor, the cotyledonoid leiomyoma or Sternberg tumor, detected incidentally in a 67-year-old woman who underwent total hysterectomy and bilateral salpingo-oophorectomy because of a persisting left ovarian cyst of 5 cm. This is the 14th case of cotyledonoid leiomyoma and 2nd case which had no intrauterine portion but had extrauterine extensions. At laparotomy, it was detected that a deep red nodular papillary tumor had been dissecting the posterior leaf of the left broad ligament, projecting into the abdominal cavity just near the left cornu of the ute

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43

Werness, Bruce A., and John G. Guccion. "Tumor of the Broad Ligament in von Hippel-Lindau Disease of Probable Mullerian Origin." International Journal of Gynecological Pathology 16, no. 3 (1997): 282–85. http://dx.doi.org/10.1097/00004347-199707000-00016.

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44

Nezhat, Farr R., Benjamin Zavala Retes, Michael P. White, Virginia Donovan, and Tanja Pejovic. "Broad ligament Extraintestinal Gastrointestinal Stromal Tumor (EGIST): Case report and brief overview of EGIST." Gynecologic Oncology Reports 33 (August 2020): 100622. http://dx.doi.org/10.1016/j.gore.2020.100622.

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45

Petkova, Kristina, and Venci Chalkov. "THE ROLE OF TUMOR MARKERS CA 125, CA 72-4 AND CA 19-9 IN DETECTION AND MONITORING OF THE COURSE OF DISEASE OF OVARIAN CARCINOMA AND CARCINOMA OF THE UTERINE BODY." Teacher of the future 31, no. 4 (2019): 931–36. http://dx.doi.org/10.35120/kij3104931p.

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Undoubtedly, nowadays the number of patients suffering from benign or malignant tumors is increasing. Particularly affected is the female population with ovarian cancer, carcinomas of the uterine body and non-inflammatory diseases of the ovary, the oviduct and the broad ligament and other benign conditions. Carcinoma is one of the most common causes of mortality in our country, as well as in the Balkans. In our country malignant tumors occupy third place in terms of total patients treated, after diseases of the respiratory and circulatory system. Due to the rapid increase in the number of pati

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Pedroso, Célia, Raquel Robalo, Pedro Sereno, Carlos Barros, and Carlos Marques. "A Rare Abdomino-Pelvic Tumor: Paraganglioma." Acta Médica Portuguesa 28, no. 1 (2015): 114. http://dx.doi.org/10.20344/amp.5403.

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<p>Paragangliomas are rare tumors, with a reported incidence of 2–8 per million. They are chromaffin cell tumors that develop from the neural crest cells and may be divided in tumors derived from the parasympathetic or sympathetic ganglia. We report a case a of a 32-year-old nulliparous woman, referred to our Infertility Clinic. Abdomino-pelvic ultrasound identified a large abdominopelvic tumor, without ovarian origin (both ovaries were identified and had normal morphology). Magnetic Resonance Imaging suggested a right adnexal multicystic, vascularized mass close to iliac vessels and que

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Rahimi, Siavash. "Concomitant Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma of the Broad Ligament and Endometrioid Endometrial Adenocarcinoma." Journal of Gynecologic Surgery 29, no. 3 (2013): 145–47. http://dx.doi.org/10.1089/gyn.2012.0102.

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Sasano, Hironobu, Shinji Sato, Akira Yajima, Jirou Akarna, and Hiroshi Nagura. "Adrenal rest tumor of the broad ligament: Case report with immunohistochemical study of steroidogenic enzymes." Pathology International 47, no. 7 (1997): 493–96. http://dx.doi.org/10.1111/j.1440-1827.1997.tb04529.x.

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Krasnopolskiy, F. "A case of uterine artery aneurysm." Journal of obstetrics and women's diseases 6, no. 3 (2020): 318–19. http://dx.doi.org/10.17816/jowd63318-319.

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The patient complains of a feeling of pulsation in the lower abdomen. When investigated in the left arch is determined by an elastic tumor, spherical, very clearly pulsating; the tumor is placed in the left broad ligament immediately above the fornix, which it protrudes from top to bottom, tightly adjoins the uterus from the place of attachment of the fornix almost to the bottom of the uterus; its size is about a hen's egg, the surface above and below is smooth, a transverse groove runs along the front surface; with prolonged pressure, the tumor decreases by half, with the cessation of pressur

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Yu, Ryan, Brigitte Courteau, Ryan Rebello, Alice Lytwyn, Monalisa Sur, and Salem Alowami. "Paravaginal female adnexal tumor of probable Wolffian origin mimicking vaginal spindle cell epithelioma on biopsy." Case Reports in Clinical Pathology 6, no. 1 (2019): 32. http://dx.doi.org/10.5430/crcp.v6n1p32.

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Female adnexal tumor of probable wolffian origin (FATWO) is a tumor of low malignant potential that arises predominantly in the broad ligament, mesosalpinx, and ovarian hilus. The rarity of FATWO increases its susceptibility to misdiagnosis as other tumors, especially when it occurs at an unusual site. We report a 29-year-old woman with a 7.2 cm left paravaginal FATWO that invaded into the vaginal lumen. The initial biopsy demonstrated features suggestive of vaginal spindle cell epithelioma, but with increased Ki67 proliferation index. Pathologists should be aware that the common sieve-like ar

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