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1. Iwahashi N, Mabuchi Y, Shiro M, Yagi S, Minami S, Ino K: Large uterine pyomyoma in a perimenopausal female: A case report and review of 50 reported cases in the literature. Mol Clin Oncol; 2016 Nov;5(5):527-531
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  • Computed tomography revealed a large unilocular mass, 50 cm in size, with an irregular surface and thickened wall, occupying the entire abdomen.
  • The resected mass was 50 cm in size and 13.5 kg in weight.
  • Although pyomyoma is a benign tumor, care must be taken to discriminate these from large abdominal tumors.

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  • (PMID = 27882238.001).
  • [ISSN] 2049-9450
  • [Journal-full-title] Molecular and clinical oncology
  • [ISO-abbreviation] Mol Clin Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Keywords] NOTNLM ; cachexia / gynecological tumor / perimenopause / pyomyoma / severe inflammatory reaction
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2. Navin P, Meshkat B, McHugh S, Beegan C, Leen E, Prins H, Aly S: Primary retroperitoneal mucinous cystadenoma-A case study and review of the literature. Int J Surg Case Rep; 2012;3(10):486-8
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  • INTRODUCTION: Primary retroperitoneal tumours of mucinous type are extremely rare and can be further sub-divided into benign, borderline or cystadenocarcinoma.
  • Abdominal examination demonstrated a mass palpable in the right iliac fossa.
  • Ultrasonography of the abdomen demonstrated a cystic mass with a magnetic resonance imaging (MRI) scan of the pelvis further defining the lesion.
  • Laparoscopy was performed to further evaluate and ultimately remove the retroperitoneal mass.
  • DISCUSSION: This is the 19th reported case of a benign primary retroperitoneal mucinous cystadenoma in the English literature.
  • CONCLUSION: Primary retroperitoneal mucinous cystadenoma is a benign tumour, however because of the malignant nature of the majority of mucinous retroperitoneal tumours they should be considered in the differential of chronic abdominal pain despite their rarity.

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  • [Copyright] Copyright © 2012 Surgical Associates Ltd. Published by Elsevier Ltd. All rights reserved.
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  • (PMID = 22809878.001).
  • [ISSN] 2210-2612
  • [Journal-full-title] International journal of surgery case reports
  • [ISO-abbreviation] Int J Surg Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
  • [Other-IDs] NLM/ PMC3421145
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3. Tang T, Johna S: Laparoscopic excision of a preperitoneal incidentaloma. JSLS; 2011 Jul-Sep;15(3):400-2
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  • BACKGROUND: Dermoid cysts are rare well-differentiated benign tumors derived from ectodermal cell origins.
  • Usually caught incidentally, they have the potential for mass effect, malignant degeneration, and rupture.
  • CASE REPORT: A 69-year-old male brought to the emergency department after a motor-vehicle accident had a preperitoneal incidental mass discovered on imaging.
  • The patient was asymptomatic from the mass, though it was expanding in size.
  • He was advised to have the mass removed, because of the possibility of malignant degeneration and rupture, and he was taken for laparoscopic surgical excision of the mass.
  • Rupture can result in a chemical granuloma when localized and can cause peritonitis when the rupture is throughout the entire abdomen.

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  • (PMID = 21985733.001).
  • [ISSN] 1086-8089
  • [Journal-full-title] JSLS : Journal of the Society of Laparoendoscopic Surgeons
  • [ISO-abbreviation] JSLS
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC3183556
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4. Zhao M, Li C, Zheng J, Yan M, Sun K, Wang Z: Cystic lymphangioma-like adenomatoid tumor of the adrenal gland: report of a rare case and review of the literature. Int J Clin Exp Pathol; 2013;6(5):943-50
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  • Adenomatoid tumors (AT) are uncommon, benign tumors of mesothelial origination most frequently encountered in the genital tracts of both sexes.
  • An abdomen computed tomography scan revealed a solitary mass in the right adrenal.
  • Grossly, the poorly-circumscribed mass measured 3.0 x 3.0 x 2.0 cm with a cut surface showing a gelatinous texture with numerous tiny cystic structures.

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  • (PMID = 23638228.001).
  • [ISSN] 1936-2625
  • [Journal-full-title] International journal of clinical and experimental pathology
  • [ISO-abbreviation] Int J Clin Exp Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC3638107
  • [Keywords] NOTNLM ; Adrenal gland / adenomatoid tumor / adrenal cyst / benign mesothelioma / immunohistochemistry / lymphangioma
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5. Maki T, Fujino S, Misu K, Kaneko H, Inomata H, Omi M, Tateno M, Nihei K: Integrally calcified solitary fibrous tumor in the retroperitoneum: a case report and review of the literature. Surg Case Rep; 2016 Dec;2(1):14
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  • A 64-year-old man presented with an incidentally detected retroperitoneal mass in the right upper abdomen.
  • Imaging tests indicated an integrally calcified mass.
  • Microscopically, the mass was mostly occupied by calcification and proliferous spindle cells were scattered with positive CD34 expression.
  • We diagnosed morphologically benign SFT and the patient remained disease-free 1 year after the excision.

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  • (PMID = 26943690.001).
  • [ISSN] 2198-7793
  • [Journal-full-title] Surgical case reports
  • [ISO-abbreviation] Surg Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  • [Other-IDs] NLM/ PMC4752942
  • [Keywords] NOTNLM ; Calcification / Retroperitoneum / Solitary fibrous tumor
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6. Agarwal AK, Kalayarasan R, Javed A, Sakhuja P: Mass-forming xanthogranulomatous cholecystitis masquerading as gallbladder cancer. J Gastrointest Surg; 2013 Jul;17(7):1257-64
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  • [Title] Mass-forming xanthogranulomatous cholecystitis masquerading as gallbladder cancer.
  • BACKGROUND: Mass-forming xanthogranulomatous cholecystitis (XGC), an uncommon inflammatory pathology of gallbladder (GB), masquerades as gallbladder cancer (GBC) and diagnosis is often a histological surprise.
  • METHODS: A retrospective analysis of prospectively collected database of patients with GB mass operated between August 2009 and September 2012 was conducted to determine clinical, radiological, and intraoperative findings that might aid in the preoperative diagnosis of mass-forming XGC and ascertain their optimal management strategy.
  • RESULTS: Of the 566 patients with GB mass and suspected GBC, 239 were found to be inoperable on preoperative workup and 129 patients had unresectable disease on staging laparoscopy/laparotomy.
  • Of these 31 patients, six with an intraoperative suspicion of benign pathology underwent cholecystectomy with segments IVb and V resection, and frozen section histopathology.
  • On computed tomography (CT) of the abdomen, continuous mucosal line enhancement and intramural hypodense bands were significantly more in Group A (p < 0.001 and 0.025).
  • While CT abdomen revealed one or more features suggestive of XGC in 64.5 % (20/31) of patients in Group A, 11(35.5 %) did not have any findings suggestive of XGC on imaging.
  • CONCLUSION: Mass-forming XGC mimics GBC, making preoperative and intraoperative distinction difficult.

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  • (PMID = 23615807.001).
  • [ISSN] 1873-4626
  • [Journal-full-title] Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract
  • [ISO-abbreviation] J. Gastrointest. Surg.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] Xanthogranulomatous cholecystitis
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7. McLoughlin LC, Davis NF, Cham A, Mohan P: Primary penile melanoma with an incidental renal oncocytoma. BMJ Case Rep; 2013;2013
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  • Preoperative staging was initiated with CT of the thorax, abdomen and pelvis.
  • A mass in the lower pole of the left kidney was found and given the presence of a primary melanoma, was highly suspicious for a metastatic deposit or a primary renal cell carcinoma.
  • A biopsy of this mass failed to give a definitive diagnosis.
  • The renal mass turned out to be a benign oncocytoma.

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  • (PMID = 24031073.001).
  • [ISSN] 1757-790X
  • [Journal-full-title] BMJ case reports
  • [ISO-abbreviation] BMJ Case Rep
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] Oncocytoma, renal
  • [Other-IDs] NLM/ PMC3794115
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8. Dahabreh MM, Hmeideen NI, Najada AS: Multicentric epithelioid hemangioendothelioma involving the lungs, trachea, liver and skeletal muscles. Respir Med Case Rep; 2012;5:20-2
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  • Epithelioid hemangioendothelioma (EH) is a rare benign vascular tumor, which typically present as multinodular lesions that can involve one organ or more.
  • Physical examination was positive for diminished breath sounds and crackles of right hemithorax, and small mass in abdominal wall.
  • CT of chest and abdomen revealed multiple nodular lesions in both lungs, liver, and right abdominal rectal muscle.

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  • (PMID = 26057597.001).
  • [ISSN] 2213-0071
  • [Journal-full-title] Respiratory medicine case reports
  • [ISO-abbreviation] Respir Med Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC3920417
  • [Keywords] NOTNLM ; Epithioid hemangioendothelioma / Lung nodules / Pulmonary hypertension
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9. Kordzadeh A: Vanek's tumour mimicking an acute appendicitis. Int J Surg Case Rep; 2011;2(8):264-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • INTRODUCTION: Vanek's tumour or Inflammatory Fibroid Polyp (IFP) are rare, benign localised lesions originating from the sub-mucosa of the gastrointestinal tract (GI) tract.(1) They have been widely reported as occurring within the stomach, Duodenum, Jejunum and Ileum, more rarely (<1%) in the caecum or appendix.
  • Subsequent, ultrasonography (USS) of the abdomen demonstrated an inflamed tubular structure originating from caecum with fluid in the pelvis mimicking an acute appendicitis.
  • Next to normal appendix an inflammatory polypoid mass was identified and on histological examination confirmed to be an IFP (Vanek's tumour).

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  • (PMID = 22096748.001).
  • [ISSN] 2210-2612
  • [Journal-full-title] International journal of surgery case reports
  • [ISO-abbreviation] Int J Surg Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
  • [Other-IDs] NLM/ PMC3215254
  • [Keywords] NOTNLM ; Appendicitis / Caecal tumour / Inflammatory fibroid polyp / Vanek's tumour
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10. Waters PS, Mitchell DP, Murphy R, McKenna M, Waldron RP: Primary malignant gastric PEComa - Diagnostic and technical dilemmas. Int J Surg Case Rep; 2012;3(2):89-91
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • He had a palpable epigatric mass on examination.
  • He underwent a CT Scan Abdomen which displayed a tumour arising from the gastric wall.
  • PEComas display a strong female predominance with a typical benign course.
  • PEComa's may be subdivided into benign, uncertain malignant potential and malignant.
  • The majority of PEComa's are benign in nature and have a better prognosis.

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  • (PMID = 22288055.001).
  • [ISSN] 2210-2612
  • [Journal-full-title] International journal of surgery case reports
  • [ISO-abbreviation] Int J Surg Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
  • [Other-IDs] NLM/ PMC3267290
  • [Keywords] NOTNLM ; Desmin / Diagnostic / Gastric / Melan-A / PEComa
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