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  Kate Glennon, Ann Treacy, Tony Geoghegan, Paul Downey, Donal Brennan
  International Journal of Gynecologic Cancer.2022; 32(4): 566.     CrossRef
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• Peritoneal HPV‐DNA test in cervical cancer (PIONEER study): A proof of concept
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  International Journal of Cancer.2021; 148(5): 1197.     CrossRef
• Cervical stromal involvement by endometrial ‘hyperplasia’: a previously unreported phenomenon with recommendations to report as stage II endometrial carcinoma
  Jennifer Taylor, W. Glenn McCluggage
  Pathology.2021; 53(5): 568.     CrossRef
• Pelvic and Ovarian Recurrence of Small HPV-associated Cervical Adenocarcinoma With Transformation to Neuroendocrine Carcinoma
  Duaa Abu-Sinn, Jackie Jamison, Matthew Evans, W. Glenn McCluggage
  International Journal of Gynecological Pathology.2021; 40(6): 541.     CrossRef
• Superficially Spreading Endocervical Adenocarcinoma in situ with Multifocal Microscopic Involvement of the Endometrial Surface: A Case Report with Emphasis on the Potential for Misdiagnosis Based on Endometrial Curettage Specimens
  Inwoo Hwang, Jiyeon Lee, Kyue-Hee Choi, Jiheun Han, Hyun-Soo Kim
  Case Reports in Oncology.2020; 13(3): 1530.     CrossRef

Peritoneal loose bodies (PLBs) are usually discovered incidentally during laparotomy or autopsy. A few cases of giant PLBs presenting with various symptoms have been reported in the literature. Here, we describe a case of a giant PLB incidentally found in the pelvic cavity of a 50-year-old man. Computed tomography revealed a free ovoid mass in the pelvic cavity that consisted of central dense, heterogeneous calcifications and peripheral soft tissue. The mass was an egg-shaped, hard, glistening concretion measuring 7.5×7.0×6.8 cm and weighing 160 g. This concretion consisted of central necrotic fatty tissue surrounded by concentrically laminated, acellular, fibrous material. Small PLBs usually do not require any specific treatment. However, if PLBs cause alimentary or urinary symptoms due to their large size, surgical removal may be recommended. It is essential for clinicians to be aware of this entity and its characteristic features to establish the correct diagnosis.

Citations

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• A Case of a Fixed Giant Peritoneal Loose Body outside the Peritoneum and near the Rectovesical Excavation
  Kotaro Nanno, Seiichi Shinji, Takeshi Yamada, Akihisa Matsuda, Ryo Ohta, Hiromichi Sonoda, Takuma Iwai, Kohki Takeda, Kazuhide Yonaga, Koji Ueda, Sho Kuriyama, Toshimitsu Miyasaka, Hiromasa Komori, Yoshinobu Shioda, Hiroshi Yoshida
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  Indian Journal of Surgery.2022; 84(1): 206.     CrossRef
• Peritoneal loose body presenting as a hepatic mass: A case report and review of the literature
  Yang Wen, Min-jie Shang, Yan-qing Ma, Song-hua Fang, Yuan Chen
  Open Medicine.2021; 16(1): 1356.     CrossRef
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  ACG Case Reports Journal.2021; 8(11): e00680.     CrossRef
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  Journal of International Medical Research.2020; 48(10): 030006052095471.     CrossRef
• A rare peritoneal egg: Case report with literature review
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• A giant peritoneal loose body impacted in the pelvic cavity, a rare and interesting finding during laparotomy
  Ayad A. Mohammed
  International Journal of Surgery: Global Health.2020; 3(6): e24.     CrossRef
• Giant Mobile Intraperitoneal Loose Body
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  ACG Case Reports Journal.2019; 6(1): e00006.     CrossRef
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• A Case of a Peritoneal Loose Body with the Maximum Diameter of 50 mm
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  Hong Zhang, Yun-zhi Ling, Ming-ming Cui, Zhi-xiu Xia, Yong Feng, Chun-sheng Chen
  World Journal of Surgical Oncology.2015;[Epub]     CrossRef

A uterus-like mass (ULM) is a central cavity lined by endometrial glands and stroma and surrounded by thick-walled smooth muscles. To date, 31 cases of ULM have been reported in the English literature. ULM typically presents as a single mass and is located in the pelvic cavity. We report here a very rare case of multiple extrapelvic ULMs involving the cecum, descending colon, and mesocolon. After extensive literature research, our case appears to be the first case of multiple ULMs found in extrapelvic sites and the first case of ULM in the colon. The present case suggests that ULM should be included in the differential diagnosis of colonic submucosal tumors in female patients with chronic abdominal pain or menstruation-associated symptoms.

Citations

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• Extrauterine adenomyoma: A case report and systematic review of the literature
  Matteo Giorgi, Luca Labanca, Gabriele Centini, Lucia Lazzeri, Francesco Giuseppe Martire, Ester Sorrentino, Virginia Mancini, Diego Raimondo, Antonio Raffone, Daniele Neola, Anna Chiara Aru, Nassir Habib, Paolo Casadio, Renato Seracchioli, Errico Zupi
  International Journal of Gynecology & Obstetrics.2024; 164(3): 869.     CrossRef
• Extrapelvic “Uterus Like Mass” Following Laparoscopic Morcellation Hysterectomy - a Consequence of Iatrogenic Implantation?
  Neha Bakshi, Shashi Dhawan
  International Journal of Surgical Pathology.2023; 31(5): 791.     CrossRef
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  Medicine.2022; 101(36): e30240.     CrossRef
• Pelvic Pain and Adnexal Mass: Be Aware of Accessory and Cavitated Uterine Mass
  Pooya Iranpour, Sara Haseli, Pedram Keshavarz, Amirreza Dehghanian, Neda Khalili, Michael S. Firstenberg
  Case Reports in Medicine.2021; 2021: 1.     CrossRef
• Endomyometriosis of the Rectum With Disseminated Peritoneal Leiomyomatosis 8 Years After Laparoscopic Myomectomy: A Case Report
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• Imaging Manifestations of Accessory Cavitated Uterine Mass—A Rare Mullerian Anomaly
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  Viola Liberale, Alessandra Surace, Lorenzo Daniele, Luca Liban Mariani
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• Extrauterine adenomyoma located in the inguinal region: a case report of a 44-year-old woman
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• Accessory and Cavitated Uterine Mass: Is It a Müllerian-Duct Anomaly?
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  Lei Liu, Hui Yang, Shu-Peng Zhang
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  International Journal of Surgical Pathology.2014; 22(5): 421.     CrossRef

Papillary thyroid carcinoma with nodular fasciitis-like stroma (PTC-NFS) is a rare variant of PTC. The term 'PTC with fibromatosis-like stroma' has been used as a synonym to describe this variant. It is characterized by extensive proliferation of fibroblasts and myofibroblasts in the tumor stroma, which occurs in up to 80% of the tumors. We herein describe a case of PTC-NFS which developed in a 49-year-old woman with the demonstration of findings of ultrasonography, fine needle aspiration cytology and histological examination of the lesion. To characterize the stromal components, we investigated the expression of several immunohistochemical markers which have been shown to be expressed differently in nodular fasciitis (NF) and fibromatosis (FM). The immunostaining results demonstrated nuclear and cytoplasmic accumulation of β-catenin, cytoplasmic transforming growth factor-β expression and nuclear Smad expression in the stromal cells, suggesting that the stromal cells in this case have similar molecular profiles to those of FM rather than NF.

Citations

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• Papillary thyroid carcinoma with desmoid-type fibromatosis: the clinicopathological features with characteristic imaging and molecular correlation requiring comprehensive treatment
  Haining Huang, Lei Li, Xiaolong Liu, Lihua Zhao, Zhihong Cui, Renya Zhang, Shuai Chen
  Human Pathology.2023; 136: 84.     CrossRef
• Papillary Thyroid Carcinoma with Desmoid-Type Fibromatosis: Review of Published Cases
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  Yoon Ah Cho, Young Lyun Oh
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• SOX11 expression in a case of papillary thyroid carcinoma with fibromatosis/fasciitis-like stroma containing BRAF c.1799_1801delTGA and CTNNB1 c.133T>C mutations
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• Papillary thyroid cancer with extrathyroidal extension of desmoid-type fibromatosis. A case report of an aggressive presentation of an uncommon pathologic entity
  Eve M. Roth, Courtney E. Barrows, Michiya Nishino, Barry Sacks, Per-Olof Hasselgren, Benjamin C. James
  International Journal of Surgery Case Reports.2019; 63: 5.     CrossRef
• Papillary thyroid carcinoma with nodular fasciitis-like stroma and β-catenin mutations should be renamed papillary thyroid carcinoma with desmoid-type fibromatosis
  Caterina Rebecchini, Antoine Nobile, Simonetta Piana, Rossella Sarro, Bettina Bisig, Sykiotis P Gerasimos, Chiara Saglietti, Maurice Matter, Laura Marino, Massimo Bongiovanni
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We present herein the occurrence of multifocal adenocarcinomas with a minute signet ring cell carcinoma that arose within a gastric inverted hyperplastic polyp (IHP) in a 40-year-old woman. Endoscopic ultrasonography demonstrated a heterogeneous hypoechoic mass in the third layer of the gastric wall. The endoscopic submucosal dissection specimen measuring 3.5×3.2×1.8 cm was a well-circumscribed protruding lesion that had a slit-shaped cavity. Histologically, the lesion consisted mainly of endophytic proliferation of hyperplastic columnar cells resembling normal foveolar epithelium. In addition, six foci of adenocarcinomas and a minute focus of signet ring cell carcinoma were randomly distributed in the superficial and deep regions. The adenocarcinoma was gradually transitioning from dysplasia, while the signet ring cell carcinoma was surrounded by hyperplastic foveolar epithelium. This is the first report of a gastric IHP with multifocal intramucosal adenocarcinomas and a signet ring cell carcinoma, and endoscopic submucosal dissection is used to completely resect it.

Citations

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• Clinicopathologic and endoscopic characteristics of ten patients with gastric hamartomatous inverted polyp: a single center case series
  Ningning Dong, Fandong Meng, Bing Yue, Junzhen Hou
  BMC Gastroenterology.2024;[Epub]     CrossRef
• Gastric hamartomatous inverted polyp: Report of three cases with a review of the endoscopic and clinicopathological features
  Takuya Ohtsu, Yu Takahashi, Mitsuo Tokuhara, Tomomitsu Tahara, Mitsuaki Ishida, Chika Miyasaka, Koji Tsuta, Makoto Naganuma
  DEN Open.2023;[Epub]     CrossRef
• Gastric Inverted Hyperplastic Polyp Removed Using Endoscopic Submucosal Dissection
  Jee Won Boo, Joon Sung Kim, Byung-Wook Kim
  The Korean Journal of Helicobacter and Upper Gastrointestinal Research.2023; 23(1): 63.     CrossRef
• The Many Faces of Gastric Inverted Polyps: a case report
  S.I. Kim, M.Y. Agapov, T.F. Savostyanov, A.A. Paratovskaya, I.A. Sokolova
  Dokazatel'naya gastroenterologiya.2023; 12(2): 88.     CrossRef
• Large gastric hamartomatous inverted polyp accompanied by advanced gastric cancer: A case report
  Gyerim Park, Jihye Kim, Sung Hak Lee, Younghoon Kim
  World Journal of Clinical Cases.2023; 11(28): 6967.     CrossRef
• Activating KRAS and GNAS mutations in heterotopic submucosal glands of the stomach
  Hourin Cho, Taiki Hashimoto, Tomoaki Naka, Yasushi Yatabe, Ichiro Oda, Yutaka Saito, Takaki Yoshikawa, Shigeki Sekine
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• Gastric Inverted Polyps—Distinctive Subepithelial Lesions of the Stomach
  Ji-Ye Kim, Soomin Ahn, Kyoung-Mee Kim, Sun Hee Chang, Han Seong Kim, Jun Haeng Lee, Jae J. Kim, Tae Sung Sohn, Hye Ju Kang, Mee Joo
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• Signet-ring Cell Carcinoma in Hyperplastic Polyp of the Stomach
  Kenta Yoshida, Tatsuya Mikami, Takao Oyama, Yuki Sato, Taro Saito, Takafumi Mikami, Chieko Itabashi, Yasushi Soma, Shinsaku Fukuda
  Internal Medicine.2019; 58(24): 3531.     CrossRef
• Inverted Hyperplastic Polyp in Stomach: A Case Report and Literature Review
  Yeon Ho Lee, Moon Kyung Joo, Beom Jae Lee, Ji-Ae Lee, Taehyun Kim, Jin Gu Yoon, Jung Min Lee, Jong-Jae Park
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• Inflammatory myofibroblastic tumor‐like stromal proliferation within gastric inverted hyperplastic polyp
  Byeong‐Joo Noh, Ji Won Min, Ji‐Youn Sung, Yong‐Koo Park, Juhie Lee, Youn Wha Kim
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• Gastric inverted hyperplastic polyp: A rare cause of iron deficiency anemia
  Jin Tak Yun, Seung Woo Lee, Dong Pil Kim, Seung Hwa Choi, Seok-Hwan Kim, Jun Kyu Park, Sun Hee Jang, Yun Jung Park, Ye Gyu Sung, Hae Jung Sul
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  Internal Medicine.2014; 53(15): 1625.     CrossRef

Renal cell carcinoma (RCC) in autosomal dominant polycystic kidney (ADPKD) is rare. To date, 54 cases of RCC in ADPKD have been reported. Among these, only 2 cases have different histologic types of RCC. Here we describe a 45-year-old man who received radical nephrectomy for multifocal RCC with synchronous papillary and clear cell histology in ADPKD and chronic renal failure under regular hemodialysis. The case reported herein is another example of the rare pathological finding of RCC arising in a patient with ADPKD.

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