Unusual uterine cervical polypoid mass presenting during pregnancy

Cytopathology ◽  
2021 ◽  
Author(s):  
Shinji Toyoda ◽  
Toshiyuki Sado ◽  
Fuminori Ito ◽  
Makiko Taniguchi ◽  
Tsunekazu Kita
Keyword(s):  
2016 ◽  
Vol 91 (4) ◽  
pp. 554-555 ◽  
Author(s):  
Gulsen Akoglu ◽  
Nazmiye Dincer ◽  
Ahmet Metin
Keyword(s):  

2021 ◽  

We presented a 60-year-old man who underwent a colonoscopy examination of a polypoid mass with a wound surface of 1.1 cm in hepatic flexure. An adenocarcinoma of intestinal type was diagnosed based on the biopsy report, and patient was referred to the hospital for colectomy. In colonoscopy and biopsy, the polypoid mass was completely removed, and despite different sections of the whole specimen in the colectomy specimen, any mass was not found, while only one out of three identified lymph nodes were involved. In laboratory tests, CBC had anemia: (Hb: 10.8 mg/ dl), elevated CEA tumor marker (range: 18 ng/ml), and lipid profile disorder together with high cholesterol (300 mg/dl), indicating colon cancer manifestation.


2020 ◽  
Vol 13 (2) ◽  
pp. 807-812
Author(s):  
Chu Van Nguyen ◽  
Huyen Thi Phung ◽  
Luan Thi Dao ◽  
Dang Hong Hai Ta ◽  
Minh Ngoc Tran

Uterine tumor resembling ovarian sex cord tumor (UTROSCT) is a rare indolent stromal neoplasm of unclear histogenesis with a distinct histopathological entity. Immunophenotypes of sex cord positivity are the most significant information to confirm the diagnosis. We present the case of a 61-year-old female with a polypoid mass in the uterus which was successfully removed by surgical resection as hysterectomy. The pathological diagnosis was UTROSCT, which was characterized microscopically by sex cord images and immunohistochemical features of calretinin, CD99, and WT1 positivity.


2012 ◽  
Vol 3 (2) ◽  
pp. 37-38
Author(s):  
Sharmin Ferdousi ◽  
SM Badruddoza

Paraganglioma or glomus tumour are named according to their origin. Jugulotympanic  paragangliomas (JTP) originates in the middle ear. There are several diagnostic pitfalls of this tumour. We now report a rare case of JTP in a 47 years old female. Pre-operative diagnosis of this case was chronic suppurative otitis media, Per-operatively it revealed an irregular     somewhat polypoid mass. On histologic examination the mass composed of nests of round to oval cells surrounded by delicate vascular septae and the diagnosis was JTP. Because JTPs are rare tumour and have variable clinical presentation & different histologic findings they are easy to misdiagnose. However this case report may help to generate awareness and to avoid misinterpretation of JTPs.   DOI: http://dx.doi.org/10.3329/akmmcj.v3i2.11693   AKMMC J 2012: 3(2): 37-38  


2001 ◽  
Vol 7 (3-4) ◽  
pp. 197-201 ◽  
Author(s):  
Robert Paczona ◽  
Laszlo Ivan ◽  
Jozsef Jori ◽  
Bela Ivanyi

Background: Giant fibrovascular polyps (FVP) are relatively rare benign neoplasm of the upper esophagus and hypopharynx. Without previous history, their diagnosis might be difficult as the endoscopic findings are sometimes misinterpretedMaterials and methods: The present report describes a case, in which the patient regurgitated his giant polypoid mass into his mouth and captured it between his teeth and buccal surface until the emergency endoscopic removalResults: After one-year of follow-up, the patient is going well, without recurrence of his polypConclusion: Although the adequate therapy for these lesions is mainly the open surgical resection, most often via cervical esophagotomy, in our case the polyp was removed successfully by peroral endoscopic operation.


2017 ◽  
Vol 11 (3) ◽  
pp. 559-563
Author(s):  
Ki Hun Lee ◽  
Sang Jin Lee ◽  
Hak Soo Kim ◽  
Sung Eun Kim ◽  
Soo Yong Choi ◽  
...  

Basaloid squamous cell carcinoma of the esophagus is very rare. Further, polypoid type of esophageal cancer is also rare. We have recently treated a case of basaloid squamous cell carcinoma which presented as a 1.3-cm esophageal polyp. A 48-year-old woman was referred to our hospital because of a polypoid mass at 36 cm distance from the upper incisor on endoscopic examination, and the result of the biopsy was basaloid squamous cell carcinoma. The patient underwent Ivor Lewis operation with lymph node dissection. Two basaloid squamous cell carcinomas, of 1.3 and 0.4 cm, were diagnosed in the final pathologic examination. Regular periodic follow-up showed no evidence of recurrence or metastasis in the 5-month postoperative period.


2009 ◽  
Vol 104 ◽  
pp. S389-S390
Author(s):  
Ravi Prakash ◽  
Nirav Shah ◽  
Roy Ferguson

2009 ◽  
Vol 59 (8) ◽  
pp. 577-582 ◽  
Author(s):  
Manabu Onodera ◽  
Yasunori Sato ◽  
Hiroko Ikeda ◽  
Yoh Zen ◽  
Seisyo Sakai ◽  
...  

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