Title Inverted Papilloma of the Renal Pelvis Associated with Renal Cell

Total Page:16

File Type:pdf, Size:1020Kb

Title Inverted Papilloma of the Renal Pelvis Associated with Renal Cell Inverted papilloma of the renal pelvis associated with renal cell Title carcinoma: a case report Ueda, Takeshi; Akimoto, Susumu; Shimazaki, Jun; Matsuzaki, Author(s) Masaru; Nagao, Kouichi Citation 泌尿器科紀要 (1992), 38(5): 561-563 Issue Date 1992-05 URL http://hdl.handle.net/2433/117552 Right Type Departmental Bulletin Paper Textversion publisher Kyoto University Acta Urol. Jpn. 38: 561-563, 1992 561 INVERTED PAPILLOMA OF THE RENAL PELVIS ASSOCIATED WITH RENAL CELL CARCINOMA: A CASE REPORT Takeshi U eda, Susumu Akimoto, J un Shimazaki, Masaru Matsuzaki* and Kouichi Nagao* From the Department of Urology, School of Medicine, Chiba University and Pathology, School of Medicine, Teikyo University, Ichihara Hospital Twenty-one cases of inverted papilloma of the renal pelvis have been described in the litera­ ture. A 71-year-old man was admitted to our hospital to examine a right renal mass. We diagnosed a right renal tumor on the basis of the findings from excretory urogram (IVP), computerized tomog­ raphy (CT) and magnetic resonance imaging (MRI). Surgical material revealed an inverted pap­ illoma in the renal pelvis. We report on the first case of an invested papilloma of the renal pelvis associated with renal cell carcinoma. (Acta Uro!. Jpn. 38: 561-563, 1992) Key words: Inverted papilloma, Renal pelvis, Renal cell carcinoma this was again demonstrated by MRI. Se­ INTRODUCTION lective arteriography showed a marked Since Potts!) reported the first case of an neovascularity in the identical portion of inverted papilloma of the urinary bladder, the kidney as mentioned above we diag­ more than 200 cases have been reported. nosed a right renal tumor. Mainly, inverted papilloma occurs in the Right nephrectomy was performed in region of the urinary trigone, bladder neck September, 1989. The weight of the right and prostatic urethra. They have been kidney was 530 g and the size was 15.0 x rarely found in the upper urinary tract. ro.O x 6.5 cm. There were two distinct Inverted papilloma is recognized as a be­ tumors in the upper portion of the kidney, nign tumor, because only 2 cases of recur­ which measured 4.0 x 5.0 x 3.0 cm and 3.5 x rence have been recorded2,3). However, a 4.0 x 3.0 cm. Another grey-colored solid few cases revealed malignant formation4 ,5) tumor, 4.0 x 2.5 x 1.0 cm, was observed in the and the coexistence of transitional cell renal pelvis (Fig. 1). Histological slides carcinoma2,6-S) We report a case of an with hematoxylin-eosin staining demon­ inverted papilloma of the renal pelvis asso­ strated that both renal tumors in the upper ciated with renal cell carcinoma. portion of the kidney were occupied by cells having a clear cytoplasm and small CASE REPORT nucleus. Pathological diagnosis was a re­ A 71-year-old man was admitted to our nal cell carcinoma, pT2NOMO. Pathologi­ hospital for examination of a renal mass cal diagnosis of the renal pelvic tumor was that was incidentally discovered by ultra­ an inverted papilloma demonstrating con­ sonography (US) during screening of the servation of the epithelial cells, seven or upper abdomen. The patient had no other eight layers of cells with no cellular dys­ urological symptoms. US demonstrated a plasia (Fig. 2). low echoic lesion of the right kidney. The postoperative course was without Cystoscopy showed a normal urothelium. any complications, and the patient has been IVP revealed distortion of the right renal receiving medication with anti-cancer drugs. pelvis. CT scan demonstrated a mass in Follow-up observation for 21 months has the upper portion of the right kidney, and shown no evidence of recurrence. 562 Acta Urol. jpn. Vol. 38, No.5, 1992 of the tumor5,12,13) One was found at autopsyl4) . The nature of inverted papilloma is con­ sidered to be that of a benign tumor. However, even if a pelvic tumor can be examined by biopsy under ureteroscopy, it is difficult to conclude that the tumor is an inverted papilloma. A biopsy specimen alone is not sufficient for distinguishing an inverted papilloma from an inverted type transitional cell carcinoma (Tee) or a combination of an inverted papilloma and Tee. There have been two reports of recurrent inverted papilloma2,3). In addi­ Fig. I. Gross specimen shows two yellowish tion there have been nine cases of inverted tumors of the upper portion and a grey­ papilloma with concomitant urothelial can­ colored tumor of the renal pelvis (ar­ 3 7 rows). cer - ,l5). These cases had malignant uro­ thelial lesions at sites independent from the inverted papilloma, but in four4- 6,15) of them carcinomas also occurred in the same lesion as the inverted papilloma. In the ;;.. present case, inverted papilloma of the renal pelvis seems to be associated with re­ nal cell carcinoma by coincidence. In any event, until now there has been no report on the coexistence of an inverted papillo­ ma of the renal pel vis and renal cell car­ cinomas. Silversteinl5) previously reported a pa­ Fig. 2. Microscopic examinations show typical tient with inverted papilloma of the left features of inverted papilloma (right. ureter after right nephrectomy for right H&E, x 25), and renal cell carcinoma renal cell carcinoma. Grainger8) demon­ with clear cytoplasm and small nucleus (left. H&E, x50). strated urothelial carcinoma in a portion of the ureteral inverted papilloma coexisting with a small renal cell carcinoma. We DISCUSSION report the first case of an inverted papil­ loma of the renal pelvis associated with More than fifty cases of inverted papillo­ renal cell carcinoma. ma of the upper urinary tract have been reported previously. Since Martz9) reported REFERENCES the first case in 1974, 22 cases including 1) Potts IF and Hirst E: Inverted papilloma ours have been identified in the renal pel­ of the bladder. j Urol 90: 175-176, 1963 VIS. Most of them had gross hematuria 2) Demeester Lj, Farrow GM and Utz DC: In­ with or without flank pain. Our case had verted papillomas of the urinary bladder. no urological symptoms and the renal Cancer 36 : 505-513, 1975 pelvic tumor was incidentally discovered at 3) Schultz RE and Boyle DE: Inverted papillo­ nephrectomy. An inverted papilloma of the ma of renal pelvis associated with contrate· renal pelvis is usually diagnosed after surgi­ ral ureteral malignancy and bladder recur­ rence . .J Urol 139: 111-113, 1988 cal treatment for a renal pelvic tumor. 5) Uyama T and Moriwaki S : Inverted papil­ Therefore, 11 of the 22 the cases underwent loma with malignant change of renal pelvis. nephroureterectomy. Six of the other cases Urology 17: 200-201, 1981 had either nephrectomylo,ll) or resection 5) Lausten GS, Anagnoataki L and Thomsen Ueda, et al.: Inverted papilloma of the renal pelvis 563 OF: Inverted papilloma of the upper urina- 1981 ry tract. Eur Urol 10: 67-70, 1984 16) Cameron KM and Lupton CH: Inverted pa- 6) Lazarevic B and Garret R : Inverted papil- pilloma of the lower urinary tract. Br J loma and papillary transitional cell carcino- Urol 48: 567-577, 1976 ma of urinary bladder report of four cases 17) Palvo DHB: Inverted papilloma of the uri- of inverted papilloma, one showing papillary nary tract. Scand J Urol Nephrol 19: 299- malignant transformation and review of the 302, 1985 literature. Cancer 42: 1904-1907, 1978 18) Watters G, Grant A, Wiley S, et al.: Invert- 7) Anderstrom C, Johanson S and Pettersson ed papilloma of the upper urinary tract. Br S: Inverted papilloma of the urinary tract. J Urol 55: 176-179, 1983 J Urol 127: 1132-1134, 1982 19) Aubert J, Dore B, Villemonteix P, et al. 8) Grainger R, Gikas GP and Grossman NB: Inverted papilloma of upper urinary tract. Urothelial carcinoma occurring with an in- Eur Urol 15: 150-152, 1988 verted papilloma of the ureter. J Urol 143: 20) Bassi P, Piazza R, Aragona F, et al.w Invert- 802-804, 1990 ed papilloma of the pelvis. Urol Int 46: 9) Matz LR, Wishart VA and Goodman MA: 73-76, 1991 Inverted urothelial papilloma. Pathology 6: 21) Arrufat JM, Vera-Roman JM, Casas V, et 37-44, 1974 al.: Papilloma invertido de ureter. Acta 10) Assor D: Inverted papilloma of the renal Urol Esp 7: 225-228, 1983 pelvis. J Urol 116: 654, 1976 22) Kunze E, Schauer A and Schmitt M: Histol- 11) Theoret G, Paquin F, Schick E, et al. In- ogy and histogenesis of two different types verted papilloma of urinary tract. Urology of inverted urothelial papillomas. Cancer 16: 149-151, 1980 51: 348-358, 1983 12) Schulze S, Holm-Nielsen A and Ravn V : 23) Taylor FM and Arroyo JG: Inverted papil- Inverted papilloma of upper urinary tract. loma of the renal pelvis: Cytologic features Urology 28: 58-61, 1986 of ureteral washings. Acta Cytol 30: 166- 13) Yamaguchi K, Yanagi S, Ito H, et al. : In- 168, 1986 verted papilloma of renal pelvis associated 24) Kyriakos M and Royce RK: Multiple simul- with transitional cell carcinoma of the blad- taneous papillomas of the upper urinary der. Urol Int 43: 302-304, 1988 tract: A case report with a review and renal 14) Stower MJ, Maciver AG, Gingell JC, et al.: pelvic inverted papillomas. Cancer 63: 386- Inverted papilloma of the ureter with ma- 380, 1989 lignant change. Br J Urol 65: 13-16, 1990 (Received on August 12, 1991 15) Silverstein SV and Carlton CE: Inverted Accepted on December 11, 1991) papilloma of ureter. Urology 17: 160-162, 和文抄録 腎 細 胞 癌 に 合 併 した 腎盂Invertedpapillomaの1例 千葉大学医学部泌尿器科学教室(主 任:島 崎 淳教授) 植 田 健*,秋 元 晋,島 崎 淳 帝京大学市原病院病理学教室(主 任 ・長尾孝一教授) 松 嵜 理**,長 尾 孝 一 腎腫 瘤 の精 査 目的 に て来 院 した71歳 男性.IVP, た.病 理 所 見 は,腎 細 胞 癌 と腎 孟invertcdpapillo- CT,MRIに て右 腎 腫 瘍 と診 断 し右 腎摘 出 術施 行 し maと の 合 併 で あ っ た.腎 孟invertedpapillomaに つ い て 若 干 の 文 献 的 考 察 を 加 え て 報 告 した.
Recommended publications
  • 8 Benign Neoplasms and Tumor-Like Lesions Roberto Maroldi, Marco Berlucchi, Davide Farina, Davide Tomenzoli, Andrea Borghesi, and Luca Pianta
    Benign Neoplasms and Tumor-Like Lesions 107 8 Benign Neoplasms and Tumor-Like Lesions Roberto Maroldi, Marco Berlucchi, Davide Farina, Davide Tomenzoli, Andrea Borghesi, and Luca Pianta CONTENTS 8.6.6 Follow-Up 131 8.7 Juvenile Angiofi broma 131 8.1 Osteoma 107 8.7.1 Defi nition, Epidemiology, Pattern of Growth 131 8.1.1 Defi nition, Epidemiology, Pattern of Growth 107 8.7.2 Clinical and Endoscopic Findings 132 8.1.2 Clinical and Endoscopic Findings 108 8.7.3 Treatment Guidelines 132 8.1.3 Treatment Guidelines 108 8.7.4 Key Information to Be Provided by Imaging 133 8.1.4 Key Information to Be Provided by Imaging 109 8.7.5 Imaging Findings 133 8.1.5 Imaging Findings 109 8.7.6 Follow-Up 141 8.1.6 Follow-Up 110 8.8 Pyogenic Granuloma 8.2 Fibrous Dysplasia and Ossifying Fibroma 110 (Lobular Capillary Hemangioma) 145 8.2.1 Defi nition, Epidemiology, Pattern of Growth 110 8.8.1 Defi nition, Epidemiology, Pattern of Growth 145 8.2.2 Clinical and Endoscopic Findings 111 8.8.2 Treatment Guidelines 145 8.2.3 Treatment Guidelines 112 8.8.3 Key Information to Be Provided by Imaging 146 8.2.4 Key Information to Be Provided by Imaging 112 8.8.4 Imaging Findings 146 8.2.5 Imaging Findings 112 8.9 Unusual Benign Lesions 147 8.2.6 Follow-Up 114 8.9.1 Pleomorphic Adenoma (Mixed Tumor) 147 8.3 Aneurysmal Bone Cyst 114 8.9.2 Schwannoma 149 8.3.1 Defi nition, Epidemiology, Pattern of Growth 114 8.9.3 Leiomyoma 150 8.3.2 Clinical and Endoscopic Findings 115 8.9.4 Paraganglioma 151 8.3.3 Treatment Guidelines 115 References 152 8.3.4 Key Information to Be Provided
    [Show full text]
  • Immune Function of Mir-214 and Its Application Prospects As Molecular Marker
    Immune function of miR-214 and its application prospects as molecular marker Qiuyuan Wang, Yang Liu, Yiru Wu, Jie Wen and Chaolai Man College of Life Science and Technology, Harbin Normal University, Harbin, China ABSTRACT MicroRNAs are a class of evolutionary conserved non-coding small RNAs that play key regulatory roles at the post-transcriptional level. In recent years, studies have shown that miR-214 plays an important role in regulating several biological processes such as cell proliferation and differentiation, tumorigenesis, inflammation and immunity, and it has become a hotspot in the miRNA field. In this review, the regulatory functions of miR-214 in the proliferation, differentiation and functional activities of immune- related cells, such as dendritic cells, T cells and NK cells, were briefly reviewed. Also, the mechanisms of miR-214 involved in tumor immunity, inflammatory regulation and antivirus were discussed. Finally, the value and application prospects of miR-214 as a molecular marker in inflammation and tumor related diseases were analyzed briefly. We hope it can provide reference for further study on the mechanism and application of miR-214. Subjects Biochemistry, Molecular Biology, Immunology Keywords miR-214, Immune cell, Tumor immunity, Inflammation, Virus, Molecular marker INTRODUCTION MicroRNAs (miRNAs) are a kind of high conserved non-coding small RNAs in evolution that bind to the 30-untranslated region (30-UTR) of target gene mRNA and regulate gene Submitted 18 September 2020 expression at post-transcriptional level. In immune responses, miRNAs act as signal- Accepted 20 January 2021 Published 16 February 2021 regulating molecules after immune-related receptors activation, and affect the expression Corresponding author of immune-related genes, thus extensively participating in various aspects of immune Chaolai Man, [email protected] response (Bosisio et al., 2019; Mehta & Baltimore, 2016).
    [Show full text]
  • A Case Report of Nasal Adenoid Cystic Carcinoma Rahim H1*, Bencheikh R2, Gliti MA1, Harmouch A3, Benbouzid MA2, Essakali L2
    Saudi Journal of Medical and Pharmaceutical Sciences Abbreviated Key Title: Saudi J Med Pharm Sci ISSN 2413-4929 (Print) |ISSN 2413-4910 (Online) Scholars Middle East Publishers, Dubai, United Arab Emirates Journal homepage: https://saudijournals.com Case Report A Case Report of Nasal Adenoid Cystic Carcinoma Rahim H1*, Bencheikh R2, Gliti MA1, Harmouch A3, Benbouzid MA2, Essakali L2 1Resident physician in otorhinolaryngology, Department of Otorhinolaryngology, Head and Neck Surgery, Ibn Sina University Hospital, Faculty of Medicine, Mohammed V University, Rabat, Morocco 2Professor of otorhinolaryngology, Department of Otorhinolaryngology, Head and Neck Surgery, Ibn Sina University Hospital, Faculty of Medicine, Mohammed V University, Rabat, Morocco 3Professor of Anatomopathology, Ibn Sina University Hospital, Faculty of Medicine, Mohammed V University, Rabat, Morocco DOI: 10.36348/sjmps.2020.v06i11.007 | Received: 22.08.2020 | Accepted: 29.08.2020 | Published: 28.11.2020 *Corresponding author: Rahim Hanaa Abstract The adenoid cystic carcinoma is a rare tumor in the region of the head and neck, it's the common malignant tumor of the salivary glands. Its location in the nasal cavity is exceptional. We report in our study a case of adenoid cystic carcinoma of the nasal cavity of a 68-year-old patient who presents nasal symptoms. The CT- scan shows a tissue process in the right nasal cavity, the endoscopy showed a process in the right nasal cavity extending to the lower cornet. The histology confirmed the adenoid cystic carcinoma. The surgical treatment consisted on the excision of the entire tumor followed by radiation therapy. Keywords: Adenoid cystic carcinoma – nasal cavity. Copyright © 2020 The Author(s): This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC BY-NC 4.0) which permits unrestricted use, distribution, and reproduction in any medium for non-commercial use provided the original author and source are credited.
    [Show full text]
  • Tumors in the Kidney (Pdf)
    Systemicist Pathology.. Lecture # 8 Title :Tumors In The Kidney Done by: Dema Mhmd Khdier A man may die, nations may rise and fall…….But an idea lives on Classification PRIMARY **Benign: 1)Papillary adenoma (in the cortex). 2)Oncocytoma 3)Medullary fibroma (interstitial cell T) **Malignant: 1)Renal cell carcinoma (most common): •Clear cell renal cell carcinoma. •Papillary renal cell carcinoma. •Chromophobe renal cell carcinoma. 2) Nephroblastoma (Wilms tumor). 3) Urothelial carcinoma of renal pelvis. SECONDARY **Benign renal tumors** _ Angiomyolipoma: Consists of vessels, smooth muscles & fat. Seen in 25-50% of patients with (Tuberous Sclerosis). **Malignant renal tumors** 1)Renal cell carcinoma (RCC) Tumors are derived from the renal tubular epithelium. • Most cases are sporadic. • 2-3% of all visceral cancers. ~85% of all renal cancer. • M:F = 2:1. Commonly 60-70 years. Risk factors 1) Smoking (most significant), obesity, HTN. 2)Unopposed estrogen Rx 3)Cadmium, petroleum products & heavy metals. 4)CRF & acquired cystic disease** (30 folds ) 5)Familial (4%) most are AD: _Von Hippel-Lindau (VHL) syndrome _Hereditary clear cell carcinoma _Hereditary papillary carcinoma Morphology of RCC Grossly: ▫ Mainly arise in cortex > polar & spherical. ▫ May extend into renal vein. ▫ Orange – yellow OR tan–brown, variegated tumor with hemorrhagic, necrotic & cystic areas. Classified according to the histological picture: 1)Clear cell carcinoma (70-80%). 2)Papillary carcinoma (10-15%). 3)Chromophobe renal carcinoma (5%). 4)Sarcomatoid carcinoma. A. Clear cell carcinoma • Most common RCC subtype. • Arise from proximal convoluted tubules. • Majority are sporadic & unilateral. • Familial forms, associated with germ-line mutation of the VHL tumor suppressor gene on 3p: *von Hippel-Lindau: rare tumor of adrenal gland tissue.
    [Show full text]
  • Analysis of the Clinical Relevance of Histological Classification of Benign Epithelial Salivary Gland Tumours
    Analysis of the Clinical Relevance of Histological Classification of Benign Epithelial Salivary Gland Tumours Hellquist, Henrik; Paiva-Correia, António; Vander Poorten, Vincent; Quer, Miquel; Hernandez- Prera, Juan C; Andreasen, Simon; Zbären, Peter; Skalova, Alena; Rinaldo, Alessandra; Ferlito, Alfio Published in: Advances in Therapy DOI: 10.1007/s12325-019-01007-3 Publication date: 2019 Document version Publisher's PDF, also known as Version of record Document license: CC BY-NC Citation for published version (APA): Hellquist, H., Paiva-Correia, A., Vander Poorten, V., Quer, M., Hernandez-Prera, J. C., Andreasen, S., Zbären, P., Skalova, A., Rinaldo, A., & Ferlito, A. (2019). Analysis of the Clinical Relevance of Histological Classification of Benign Epithelial Salivary Gland Tumours. Advances in Therapy, 36(8), 1950-1974. https://doi.org/10.1007/s12325-019-01007-3 Download date: 01. okt.. 2021 Adv Ther (2019) 36:1950–1974 https://doi.org/10.1007/s12325-019-01007-3 ORIGINAL RESEARCH Analysis of the Clinical Relevance of Histological Classification of Benign Epithelial Salivary Gland Tumours Henrik Hellquist . Anto´nio Paiva-Correia . Vincent Vander Poorten . Miquel Quer . Juan C. Hernandez-Prera . Simon Andreasen . Peter Zba¨ren . Alena Skalova . Alessandra Rinaldo . Alfio Ferlito Received: May 2, 2019 / Published online: June 17, 2019 Ó The Author(s) 2019 ABSTRACT to investigate whether an accurate histological diagnosis of the 11 different types of benign Introduction: A vast increase in knowledge of epithelial salivary gland tumours is correlated to numerous aspects of malignant salivary gland any differences in their clinical behaviour. tumours has emerged during the last decade Methods: A search was performed for histolog- and, for several reasons, this has not been the ical classifications, recurrence rates and risks for case in benign epithelial salivary gland malignant transformation, treatment modali- tumours.
    [Show full text]
  • Upper Urinary Tract Inverted Papillomas: Report of 10 Cases
    ONCOLOGY LETTERS 4: 71-74, 2012 Upper urinary tract inverted papillomas: Report of 10 cases JIN-DAN LUO, PING WANG, JUN CHEN, BEN LIU, SHUO WANG, BO-HUA SHEN and LI-PING XIE Department of Urology, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, P.R. China Received February 21, 2012; Accepted April 20, 2012 DOI: 10.3892/ol.2012.706 Abstract. The aim of the study was to review the clinical at The First Affiliated Hospital of Zhejiang University, China, features and treatments of 10 (9 males and 1 female; age range, and reviewed the clinical syndromes, diagnostic procedures, 61-73 years; median age, 67 years) upper urinary tract inverted treatment approaches and follow-up study results of each papilloma (IP) cases between 1995 and 2010. The clinical patient. syndromes, diagnostic procedures, treatments and results of the follow-up were evaluated. The results showed that the site Patients and methods of tumor development was the ureter in 6 cases and the renal pelvis in 4 cases. It was also identified that 7 tumors devel- The present study included 10 pa tients who had been hospital- oped on the left side and 3 developed on the right side of the ized in our Department of Urology between 1995 and 2010 as ureter and renal pelvis, respectively. A nephroureterectomy was a result of IP within the upper urinary tract. Of the 10 patients, performed in the first 6 cases, while a partial ureterectomy was 9 were male and 1 was female (age range, 61-73 years; median, performed in 3 cases and a local resection was performed endo- 67 years).
    [Show full text]
  • Inverted Urothelial Papilloma of the Upper Urinary Tract: Description of Two Cases with Systematic Literature Review R
    Santi et al. Diagnostic Pathology (2020) 15:40 https://doi.org/10.1186/s13000-020-00961-9 RESEARCH Open Access Inverted urothelial papilloma of the upper urinary tract: description of two cases with systematic literature review R. Santi1, I. C. Galli2, V. Canzonieri3,4, J. I. Lopez5 and G. Nesi2* Abstract Background: Inverted urothelial papilloma (IUP) of the upper urinary tract is an uncommon benign tumour that occasionally presents as a polypoid mass causing urinary obstruction. Histologically, IUP is characterised by a proliferating urothelium arranged in cords and trabeculae, in continuity with overlying intact epithelium, and extending into the lamina propria in a non-invasive, endophytic manner. Cytological atypia is minimal or absent. Top differential diagnoses include urothelial carcinoma with inverted growth pattern and florid ureteritis cystica. Although urothelial carcinomas of the upper urinary tract with prominent inverted growth pattern commonly harbour microsatellite instability, the role of the mutator phenotype pathway in IUP development is still unclear. The aim of this study was to describe two additional cases of IUP of the upper urinary tract, along with an extensive literature review. Case presentation: We observed two polypoid tumours originating in the renal pelvis and the distal ureter, respectively. Both patients, a 76-year-old woman and a 56-year-old man, underwent surgery because of the increased likelihood of malignancy. Histology was consistent with IUP and patients are alive and asymptomatic after long-term follow-up (6 years for the renal pelvis lesion and 5 years for the ureter lesion). The tumours retained the expression of the mismatch-repair protein MLH1, MSH2, and PMS2 whereas loss of MSH6 was found in both cases.
    [Show full text]
  • Papillary Mucinous Adenocarcinoma of the Endolymphatic Sac: a Rare Middle Ear Neoplasm
    Open Access Case Report DOI: 10.7759/cureus.16413 Papillary Mucinous Adenocarcinoma of the Endolymphatic Sac: A Rare Middle Ear Neoplasm Muhammad Tahir 1, 2 , Cherish Frick 3 , Ghassan Tranesh 4 1. Pathology and Laboratory Medicine, University of South Alabama Hospital, Mobile, USA 2. Pathology, Case Western Reserve University School of Medicine, Cleveland, USA 3. Surgery, Lancaster General Hospital, Pennsylvania College of Health Science, Lancaster, USA 4. Anatomical and Clinical Pathology, University of Arizona, Tucson, USA Corresponding author: Muhammad Tahir, [email protected] Abstract Glandular neoplasms of the temporal-mastoid region and endolymphatic sac (ELS) are rare, and it is quite challenging to differentiate between an adenoma and an adenocarcinoma. ELS tumors (ELST) usually present with papillary, follicular, or solid patterns and can be further distinguished histologically and through immunohistochemistry. The microscopic features and clinical course of this neoplasm have been comprehensively explained by Heffner, who considered it “low-grade adenocarcinoma of likely ELS origin.” The papillary form more commonly affects females, and it is a more aggressive form of ELST that is destructive and exhibits extensive local spread. The tumor usually has a close association with von Hippel- Lindau (VHL) disease, but 11%-30% of the ELST cases develop in individuals without a VHL mutation. ELSTs manifest with headaches, hearing loss, ear discharge, and cranial nerve palsies. Currently, the only available curative therapeutic intervention consists of wide local excision and long-term follow-up. Because of the sensitive location of this tumor, the adjuvant radiotherapy options are still questionable. In this case report, the author presents a 74-year-old woman with a past medical history of Schneiderian papilloma and was diagnosed with papillary mucinous adenocarcinoma of the ELS not associated with VHL disease.
    [Show full text]
  • Benign Diseases of the Urinary Tract at CT and CT Urography
    Abdominal Radiology (2019) 44:3811–3826 https://doi.org/10.1007/s00261-019-02108-x SPECIAL SECTION : UROTHELIAL DISEASE Benign diseases of the urinary tract at CT and CT urography Kimberly L. Shampain1,2 · Richard H. Cohan1 · Elaine M. Caoili1 · Matthew S. Davenport1 · James H. Ellis1 Published online: 24 June 2019 © Springer Science+Business Media, LLC, part of Springer Nature 2019 Keywords CT urography · Genitourinary tract · Benign urinary tract lesions Introduction Distinctive‑appearing benign urinary tract pathology There are many benign conditions that can afect the urinary tract. With respect to CT urography, these can be divided Upper and lower tract into two broad groups: (1) abnormalities that often have a distinctive appearance and (2) abnormalities that may be Pyeloureteritis and cystitis cystica mistaken for urothelial cancers. This article will illustrate the CT or CT urographic appearance of some of the many Pyeloureteritis cystica and cystitis cystica are benign urinary benign urinary tract lesions. When applicable, the article tract abnormalities, with cystitis cystica being more com- will provide explanations as to how to minimize the likeli- mon. The process, which is felt to be secondary to chronic hood that benign but clinically relevant entities will go unde- urothelial infammation, consists of glandular metaplasia of tected during the search for common causes of hematuria submucosal cysts (von Brunn nests), which enlarge within (stones, renal cancers, and urothelial neoplasms) and will the wall of the urothelium and then project into the lumen provide information as to how some patients with cancer of the urothelium. Most afected patients have a history of mimics can have suggestive clinical presentations or CT urinary tract infections and urolithiasis.
    [Show full text]
  • The Role of Human Papilloma Virus in Urological Malignancies
    ANTICANCER RESEARCH 35: 2513-2520 (2015) Review The Role of Human Papilloma Virus in Urological Malignancies ISABEL HEIDEGGER1, WEGENE BORENA2 and RENATE PICHLER1 1Department of Urology and 2Division of Virology, Department of Hygiene, Microbiology and Social Medicine, Medical University Innsbruck, Innsbruck, Austria Abstract. Human papillomavirus (HPV) is associated with reading frames encode early (E) and late (L) genes required cancer of the cervix uteri, penis, vulva, vagina, anus and for viral genome replication (5,6). Among them E6 and E7 oropharynx. However, the role of HPV infection in urological are the major oncoproteins altering the function of critical tumors is not yet clarified. HPV appears not to play a major host cellular proteins. HPV E6 leads to the degradation of causative role in renal and testicular carcinogenesis. the tumor suppressor p53, while HPV E7 degrades the tumor However, HPV infection should be kept in mind regarding suppressor RB (7) (Figure 1). cases of prostate cancer, as well as in a sub-group of patients In generally, HPVs cause different types of diseases with bladder cancer with squamous differentiation. ranging from benign lesions to invasive tumors (8). Mucosal Concerning the role of HPV in penile cancer incidence, it is HPVs are distinguished by their potential to cause malignant a recognized risk factor proven in a large number of studies. progression: Low-risk HPVs (types 6, 11, 40, 42, 43, 44, 54, This short review provides an update regarding recent 61, 70, 72 and 81) which cause low-grade lesions such as literature on HPV in urological malignancies, thereby, also benign warts, respiratory papillomas, as well as a proportion discussing possible limitations on HPV detection in of low-grade cervical intra-epithelial neoplasms, vulvar and urological cancer.
    [Show full text]
  • Modern Pathology
    VOLUME 32 | SUPPLEMENT 2 | MARCH 2019 MODERN PATHOLOGY 2019 ABSTRACTS GENITOURINARY PATHOLOGY (INCLUDING RENAL TUMORS) (776-992) MARCH 16-21, 2019 PLATF OR M & 2 01 9 ABSTRACTS P OSTER PRESENTATI ONS EDUCATI ON C O M MITTEE Jason L. Hornick , C h air Ja mes R. Cook R h o n d a K. Y a nti s s, Chair, Abstract Revie w Board S ar a h M. Dr y and Assign ment Co m mittee Willi a m C. F a q ui n Laura W. La mps , Chair, C ME Subco m mittee C ar ol F. F ar v er St e v e n D. Billi n g s , Interactive Microscopy Subco m mittee Y uri F e d ori w Shree G. Shar ma , Infor matics Subco m mittee Meera R. Ha meed R aj a R. S e et h al a , Short Course Coordinator Mi c h ell e S. Hir s c h Il a n W ei nr e b , Subco m mittee for Unique Live Course Offerings Laksh mi Priya Kunju D a vi d B. K a mi n s k y ( Ex- Of ici o) A n n a M ari e M ulli g a n Aleodor ( Doru) Andea Ri s h P ai Zubair Baloch Vi nita Parkas h Olca Bast urk A nil P ar w a ni Gregory R. Bean , Pat h ol o gist-i n- Trai ni n g D e e p a P atil D a ni el J.
    [Show full text]
  • Site Diagnosis Cardiovascular System 659 Heart: 1 Atrial Myxoma 1 Artery
    Stony Brook BioBank Specimen Collection (updated 2/11/16) Site Diagnosis Cardiovascular 659 System Heart: 1 Atrial myxoma 1 Artery: 5 Normal 5 Blood: 652 Vein: 1 Leiomyosarcoma well-differentiated (inferior vena cava) 1 Digestive System 508 Appendix: 3 Normal and benign 3 Colon: 242 Adenocarcinoma 74 Adenoma (adenomatous polyp) 14 Crohn's disease 5 Diverticulitis 2 High grade sarcoma/liposarcoma 1 Metastatic poorly differentiated carcinoma 3 Ulcerative Colitis 2 Normal and benign 141 Duodenum: 5 Adenocarcinoma (including signet-ring cell features) 3 Adenomatous polyp 1 GIST 1 Esophagus: 17 Adenocarcinoma 4 Squamous cell carcinoma 2 Normal and benign 11 Gallbladder: 2 Normal and benign 2 Adenocarcinoma (15, including 3 samples with Liver: 35 18 colorectal primary) Cirrhosis 1 Hepatoblastoma 1 Hepatocellular carcinoma 2 Metastatic leiomyosarcoma 1 Normal and benign 12 Parotid: 22 Adenocarcinoma 1 Adenoid cystic carcinoma 1 Cellular pleomorphic adenoma 1 Follicular lymphoma 1 Keratinized squamous cell carcinoma 2 Neuroendocrine carcinoma 1 Warthin's tumor 6 Normal and benign 9 Pancreas: 60 Adenocarcinoma 23 Carcinoid tumor 1 Carcinoma (NOS) 2 Chronic pancreatitis 1 Diffuse large B cell lymphoma 1 Intraductal papillary mucinous neoplasm (IPMN) 2 Microcystic adenoma 1 Mucinous cystadenoma 1 Neuroendocrine tumor 1 Tubulovillous Adenoma of Ampulla of Vater 1 Normal and benign 26 Rectum: 23 Adenocarcinoma 6 Adenoma 1 GIST 1 Invasive squamous cell carcinoma 2 Spindle cell lesion with extensive necrosis 3 Retroperitoneum 4 Fibromatosis 1 Liposarcoma
    [Show full text]