• Title/Summary/Keyword: Cystadenocarcinoma

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A Case of Cystadenocarcinoma Misdiagnosed as a Benign Tumor (양성 종양으로 오인된 낭선암종 1례)

  • Hwang, So-Min;Lee, Jong Seo;Kim, Hyung Do;Jung, Yong Hui;Kim, Hong Il
    • Archives of Craniofacial Surgery
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    • v.14 no.2
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    • pp.124-128
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    • 2013
  • Cystadenocarcinoma of the salivary gland is a rare malignant tumor. It was first defined as papillary cystadenocarcinoma in the 1991 World Health Organization (WHO) classification, and it was reclassified as cystadenocarcinoma in the 2005 WHO classification. It is a low-grade neoplasm that features slow growing and predominantly cystic growth. We report a case of cystadenocarcinoma occurring on the parotid gland of a 61-year-old female patient presenting palpable mass on her left cheek. Preoperative examination may not reveal typical malignant characteristics. Such as in our case, the differential diagnosis between cystadenocarcinoma and benign lesion is difficult occasionally. We discuss the clinical and histopathological features of cystadenocarcinoma with the review of the literature.

MRI findings of a huge cystadenocarcinoma of the palate (구개에 발생한 거대 낭샘암종의 MRI 소견)

  • Choi, Jin-Woo
    • Imaging Science in Dentistry
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    • v.40 no.4
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    • pp.191-196
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    • 2010
  • Cystadenocarcinoma of the salivary glands is a very rare, slow growing, and low-grade malignant neoplasm. It is characterized by predominantly cystic growth with or without the intraluminal papillary component. However, it lacks of any additional specific histopathologic features that characterize other types of salivary carcinomas showing cystic growth. Therefore, definite diagnosis of the cystadenocarcinoma is difficult and it is often misdiagnosed. It is conceptually the malignant counterpart of the benign cystadenoma. We present a cystadenocarcinoma on the palate of a 49-year-old man with special emphasis on magnetic resonance imaging.

Differential Diagnosis of Ovarian Mucinous, Serous, and Endometrioid Adenocarcinoma in Peritoneal Washing Cytology (복막세척액 세포검사에서 난소의 점액성, 장액성 및 자궁내막양 선암종의 감별진단)

  • Lee, Shi-Nae;Park, In-Ae
    • The Korean Journal of Cytopathology
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    • v.11 no.2
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    • pp.83-88
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    • 2000
  • This study presents the cytologic features of peritoneal washings, with particular emphasis on the cytologic discrimination among serous, mucinous, and endometrioid adenocarcinoma of the ovary. We selected histologically confirmed 27 cases of peritoneal washing : 8 cases of serous cystadenocarcinomas, 5 cases of mucinous cystadenocarcinomas, and 14 cases of endometrioid adenocarcinomas. The most frequent cytologic pattern of three tumors was clusters. Ball pattern was found in serous cystadenocarcinoma(36%) and acinar pattern in endometrioid adenocarcinoma(36%). Mucinous adenocarcinoma showed mucoid background(100%) and endometrioid adenocarcinoma revealed inflammatory background(43%). The cytoplasmic vacuoles were noted in 80%, 13%, and 43% of mucinous, serous, and endometriold adenocarcinoma, respectively. The endometrioid adenocarcinoma showed prominent nucleoli(64%). In conclusion, the cytologic findings of mucinous cystadenocarcinoma were different from that of serous and endometrioid carcinomas, such as mucoid background, abundant cyytoplasm with vacuolated cytoplasm, and peripherally located cytoplasm. Although endometriold carcinoma showed acinar pattern and prominent nucleoli, the differential diagnosis between serous cystadenocarcinoma and endometrioid adenocarcinoma in peritoneal washing cytology was was always possible.

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A Case of Ovarian Serous Cystadenocarcinoma Diagnosed by Cervicovaginal Smear (자궁경부.질도말로 진단된 난소의 장액성 낭성암종 1예)

  • Park, Hye-Rim;Nam, Joo-Hyun;Park, Young-Euy
    • The Korean Journal of Cytopathology
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    • v.3 no.2
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    • pp.104-110
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    • 1992
  • Although there have been a few reports of cases in which cancer cells of extrauterine origin were observed in vaginal smears, such findings are relatively uncommon. We recently experienced a case of ovarian serous cystadenocarcinoma diagnosed by cervicovaginal smear in a 56-year-old woman in routine work-up of carcinoma peritonei. The cellular features were several scattered cellular clusters of adenocarcinoma cells in clear background without tumor diathesis. Psammoma body was not present. Exploratory laparotomy confirmed the diagnosis of bilateral ovarian serous cystadenocarcinoma with multiple metastases.

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Cystadenocarcinoma Arising from Submandibular Gland (악하선에 발생한 낭샘암종)

  • Park, Ji Su;Koo, Bon Seok
    • Korean Journal of Head & Neck Oncology
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    • v.31 no.2
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    • pp.46-48
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    • 2015
  • Cystadenocarcinoma of salivary gland is an rare, slow-growing, low-grade malignant neoplasm characterized by cysts and papillary endocystic projections. Major locations of this tumor are parotid glands, and minor salivary glands, while occurrence in submandibular gland is extremely rare. Only few cases have been reported in the literatures. Cystadenicarcinoma behaves in an indolent manner and recurrence is rarely occured, surgical complete excision is considered treatment of choice. We experienced a case of cystadenocarcinoma arising from submandibular gland, so we report this case with a review of literature.

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Renal Rupture by Cystadenocarcinoma in a Yorkshire Terrier

  • Choi, Ji-Hye;Kim, Jin-Kyung;Jang, Jae-Young;Kim, Hyun-Wook;Kim, Jun-Young;Yoon, Jung-Hee
    • Journal of Veterinary Clinics
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    • v.25 no.3
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    • pp.224-226
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    • 2008
  • A 13-year-old, spayed female, Yorkshire terrier was presented with a history of vomiting and diarrhea. Radiographic and ultrasonographic studies suggested rupture of right renal cyst. Left kidney had increased cortical echogenecity with indistinct corticomedullary junction on sonogram. Unilateral nephroureterectomy of right kidney was performed. Histopathologic examination of the resected renal mass confirmed a renal cystadenocarcinoma. To the best of our knowledge, it is the first case report of renal cystadenocarcinoma in a small breed dog in Korea.

MR Imaging of Primary Retroperitoneal Mucinous Cystadenocarcinoma in Pregnant Woman (임산부에서 발생한 원발성 후복막 점액낭샘암종의 자기공명영상 소견: 1예 보고)

  • Lee, Jisun;Cho, Bum Sang;Kim, Yook;Yi, Kyung Sik;Kang, Min Ho;Lee, Seung Young;Kim, Sung Jin;Park, Kil Sun
    • Investigative Magnetic Resonance Imaging
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    • v.17 no.3
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    • pp.243-248
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    • 2013
  • Primary retroperitoneal mucinous cystadenocarcinoma is a very rare malignancy. To date, 51 cases have been reported, including 3 in pregnant women. Herein, we report magnetic resonance findings of a 31-year-old Korean woman (15 weeks and 3 days pregnant) with primary retroperitoneal mucinous cystadenocarcinoma. On abdominal magnetic resonance imaging (MRI), a mass was identified in the retroperitoneal area with a nodular lesion showing heterogeneous signal intensity and focal wall thickening on T1- and T2-weighted images. Exploratory laparotomy and tumor excision were performed. Histological examination revealed primary retroperitoneal mucinous cystadenocarcinoma. The patient subsequently underwent total hysterectomy, bilateral salpingo-oophorectomy, and omentectomy for metastatic mucinous cystadenocarcinoma of both ovaries 15 months after her initial surgery.

Cystadenocarcinoma in the Ovary of Thoroughbred Mare

  • Son, Young-Sook;Lee, Choung-Seop;Jeong, Won-Il;Hong, Il-Hwa;Kim, Young-Kyun;Kwon, Oh-Deok;Jeong, Kyu-Shik
    • Proceedings of the Korean Society of Veterinary Pathology Conference
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    • 2003.10a
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    • pp.55-55
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    • 2003
  • Papillary cystadenocarcinoma is an uncommon ovarian neoplasm of domestic animals, with the possible exception of the bitch. In the horse ovary, it is rare as compared with benign epithelial tumors. This case reports the gross and histopathological finding of cystadenocarcinoma in a 10-year-old, clinically healthy Thoroughbred mare. (omitted)

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A Case of Mucinous Cystadenocarcinoma in Labial Mucosa of Upper Lip (상순 구순점막에 발생한 점액낭선암종 1예)

  • Um, Jung Hwan;Jo, Dong In;Kim, Soon Heum
    • Korean Journal of Head & Neck Oncology
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    • v.37 no.1
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    • pp.43-46
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    • 2021
  • Mucinous cystadenocarcinoma (MCA) is a malignant tumor that mainly occurs in the breast or ovary, but MCA is internationally rarely reported in head and neck region. Especially MCA in minor salivary gland of oral cavity is even more rare. It is characterized by cystic spaces lining of epithelial cells containing intracytoplasmic mucin. We report a case of MCA in the labial mucosa of upper lip considered to develop from minor salivary gland with a review of literatures.