- Case report
- Open Access
Diffuse and multifocal nephrogenic adenoma with Familial Mediterranean Fever: a case report with molecular study
© Ishikawa et al. 2015
Received: 22 March 2015
Accepted: 8 July 2015
Published: 16 July 2015
Nephrogenic adenoma, also referred to nephrogenic metaplasia, is a benign proliferative lesion of urothelium, usually associated with chronic physical stimuli or inflammation. Familial Mediterranean fever is an inherited autosomal recessive disease characterized by recurrent short episodes of fever. The site of mutation is found in MEFV gene which controls inflammatory responses. We have experienced a case of nephrogenic adenoma in a 16-year-old girl with Familial Mediterranean Fever, showing proliferative lesions diffusely in the urinary bladder and multifocally in the other parts of urinary tract. These lesions disappeared after colchicine treatment. We searched for MEFV gene mutation using the specimen from the resected urinary bladder and detected heterozygous mutation of E148Q. There is a possibility that control of inflammation caused by the surgery for vesicoureteral reflux in the local site didn’t work well on the background of heterozygous mutation of MEFV gene, and as a result, nephrogenic adenoma appeared. This is the first report of a combination of two rare diseases. We have to be aware that nephrogenic adenoma can occur in association with Familial Mediterranean Fever, and the former condition should be taken into consideration when rendering a correct pathological diagnosis.
Nephrogenic adenoma is a benign tumor-like lesion of the urinary tract, characterized by a papillary and tubular proliferation of cuboidal cells similar to the epithelial cells of distal renal tubules. It occurs anywhere in the urinary tract, but it is most frequently found in the bladder . It was first described in 1949 by Davis , and originally thought to arise from a remnant of mesonephric tissue or metaplasia of the urothelium in response to chronic irritation and mucosal damage. Currently, it is known that exfoliated and implanted renal tubular cells into the urinary tract mucosa form the disease . The most common histological pattern is a proliferation of small tubules composed of a single layer of cuboidal epithelium. These tubules are often surrounded by a hyalinized basement membrane and contain blue mucin in the lumens. It may also grow in papillary, cystic or solid pattern. Hobnail cells may be seen in papillary growth areas. In cystic pattern, colloid-like eosinophilic secretion or blue-tinged mucin is frequently observed . Occasionally, clear cells or signet-ring cells can be seen in solid area, which could be confused with poorly differentiated adenocarcinoma. Although it arises commonly in adults, approximately 10 % of the patients are children, and several cases of even younger patients have been reported in the literature [4–7].
Familial Mediterranean fever (FMF) was first reported as ‘benign paroxysmal peritonitis’ in 1945  and the current name of the disease was proposed in 1958 . Most of the reported cases are autosomal recessive disease characterized by recurrent short episodes of fever and pain due to serosal inflammation . In 1997, a responsible gene was cloned and named MEFV. It encodes a protein pyrin that controls inflammation [11, 12]. Frequent mutations have been found in M694V, M694I, V726A, M680I of exon10 and, E148Q of exon 2 . This disease is most common in the periodic fever syndrome and characterized by high effectiveness of colchicine administration . We present the first rare case of nephrogenic adenoma secondary to FMF, occurring throughout the urinary tract. There has been no such a report in the literature and also, it is very rare that nephrogenic adenoma involves almost the whole mucosa of urinary tract.
A 16-year-old girl presented with disturbed consciousness and was admitted to our hospital under the diagnosis of hypertonic dehydration. During the pregnancy (32 weeks of gestational age) of her mother (29-year-old at that time), she was born by an urgent cesarean section for a shock state due to rupture of the right ovary metastasized by gastric cancer. The mother died of gastric cancer at the age of 33. The patient presented with fetal distress syndrome at birth, and thereby had sequelae such as developmental and mental retardation and epilepsy. Thereafter, she repeated urinary tract infection (UTI) caused by vesicoureteral reflux. However, even after the surgery, remittent fever came to arise twice or three times a month, but causative bacteria could not be identified by either urinalysis or urine culture. Leukocytosis and slightly high level of CRP (C-reactive protein) continued to be observed. Immunological test revealed slightly low value of CH50. On admission, swelling of left kidney was pointed out with the abdominal computed tomography. Abdominal ultrasonography revealed the left hydroureteronephrosis associated with a bladder mass. In the meantime, the tumor gradually enlarged to fill the whole lumen of the bladder, and she finally developed bilateral hydroureteronephrosis. As a result, the patient underwent total cystectomy followed by cutaneous ureterostomy.
Summary of antibodies employed in this case
Anti-Human Cytokeratin 7, monoclonal, Clone OV-TL 12/30
Dako, Glostrup, Denmark
Anti-Human P504S, rabbit monoclonal, Clone 13H4
Dako, Glostrup, Denmark
Anti-CA19-9, mouse monoclonal, Clone BC/121SLE
Biocare, Concord, USA
Anti-Vimentin, mouse monoclonal, Clone V9
Dako, Glostrup, Denmark
Anti-Human CD138, monoclonal, Clone MI15
Dako, Glostrup, Denmark
Anti-CD10, rabbit monoclonal, Clone SP67
Roche, Basel, Switzerland
Anti-p63, mouse monoclonal, Clone BC4A4
Biocare, Concord, USA
Anti-Human Prostate-Specfic Antigen, Clone ER-PR8
Dako, Glostrup, Denmark
Anti-Pax8, mouse monoclonal, Clone BCl2
Biocare, Concord, USA
Anti-Pax2, rabbit monoclonal, Clone EP3251
Abcam, Cambridge, UK
Anti-Ki67, rabbit monoclonal, Clone 30-9
Roche, Basel, Switzerland
Considering the effectiveness of colchicine treatment, we searched for MEFV gene mutations. In Japan, about 100 cases of FMF have been reported with frequent mutations found in E148Q (exon2) and M694I (exon10), so we searched for these mutations using formalin fixed samples of this case. Genomic DNA was extracted from 10 FFPE sections of 10 μm thickness using QIAamp DNA FFPE tissue kit (QIAGEN, Venio, Netherland) according to the manufacturer’s recommendations. The following PCR primers were used for amplification of MEFV (exon2 and, exon10).
5’-AAAGAGCAGCTGGCGAATGT-3’ (exon 10-R).
In the past, nephrogenic adenoma was thought to arise from the remnant of embryogenic mesonephric tissue in the urinary tract, or from metaplastic change of urothelium due to inflammation or injury. In 1981, Bhagavan et al. examined nephrogenic adenoma morphologically with electron microscopy and found the presence of Tamm-Horsfall protein . They revealed that this lesion was of mesonephric origin rather than of metanephric. Based on the fact that the nephrogenic adenoma often occurs in patients who received kidney transplantation, Mazal et al. in 2002  made a research into the origin of nephrogenic adenoma. They analyzed X and Y chromosomes employing fluorescence in situ hybridization. In the cases of male recipients from female donors, the cells of nephrogenic adenoma had XX chromosome pattern, On the contrary, in the cases of female recipients from male donors, the cells had XY chromosome pattern. These results indicated that origin of nephrogenic adenoma was donor-derived renal cells . Moreover they thought nephrogenic adenoma in extrarenal organs like urinary bladder was caused by proliferation of cells of renal origin, and showed positive immunostaining of PAX2 . PAX2 is a transcriptional factor in development and expressed in renal tubular cells and parietal cells of the Bowman’s capsule of gromerulus . PAX2 has recently been considered to be one of the useful markers for nephrogenic adenoma . “ PAX8, another transcriptional factor, expressed in renal cells is also positive in nephrogenic adenoma . It is currently thought that dislodged renal tubular epithelial cells are transplanted into the urinary tract mucosa and engraftment occurs, resulting in the disease . In the present case, repeated urinary tract infection might have contributed to the development of nephrogenic adenoma. We consider that occurrence of the tumor in renal pelvis of both sides after bladder extraction supported this hypothesis.
About 10 % of the cases with nephrogenic adenoma occur in pediatric age , and show the same morphological and immunohistochemical features as adult cases . They occur under the specific pathological conditions such as Turner's syndrome  or prune belly syndrome . Multifocal  and/or diffuse  lesions have also been reported. FMF is known to cause inflammatory conditions such as peritonitis, pleurisy, arthritis, erysipelas-like erythema and pericarditis. Responsible gene of FMF located at chromosome 16p13.3 encodes a pyrin/marenostrin protein composed of 781 amino acids and consists of 10 exons [11, 12]. Usually, pyrin has N-terminal PYRIN domain and C-terminal B30.2 domain. Activity of caspase-1 is regulated by ASC (apotosis-associated speck-like protein which contains a caspase recruitment domain) which bound to PYRIN domain and, B30.2 domain also regulates activity of IL-1β by directely inhibition of caspase-1 activation [19, 20]. Major mutations of FMF are found in E148Q in exon 2, and M894V, M694I, V726A, and M680I in exon 10 of PYD [21, 22]. If there is a mutation in exon 10, the diagnosis of FMF can be confirmed. Additionally, if mutations in the other exons, including heterozygous mutation are detected, colchicine can be utilized not only for a treatment, but also for a diagnosis of FMF variant . In FMF variants, mutations in exon 1 (E84K), exon 2 (L110P, E148Q, R202Q, G304R), exon 3 (P369S, R408Q) and exon5 (S503C) are known. It is believed that inflammation is provoked by missense mutations of PYRIN gene which result in loss of suppressive function of inflammasome and increase of IL-1β production [19, 20]. In our case, only one heterozygous mutation of E148Q (exon2) was observed. There is a report that this mutation was seen in 20 % of Japanese patients , but the present case was diagnosable as FMF variant, because treatment with colchicine was very effective. We did not search for other mutations on the chromosome, because most of them are limited at E148Q (exon2) and, M694I (exon 10) in the Japanese patients. Pyrin, located in microtubules and actin , is a protein highly expressed in white blood cells. They are coded by MEFV gene which regulates inflammatory response by interacting with the cytoskeletons and mutation of this gene probably decreased or deleted its function . Colchicine also has a function to inhibit the polymerization of microtubules (tubulin). In the present case, not only white blood cells but also the tumor cells of nephrogenic adenoma were positive for vimentin. This suggests the possibility of expression of tubulin (component of cytokelaton). Many of the FMF cases are autosomal recessive, and the symptoms are less likely to occur in heterozygous mutation of E148Q (exon 2), so that the patient might have different mutations to cause the symptoms.
To our knowledge, this is the first report of nephrogenic adenoma in a FMF patient. We speculate that control of inflammation in the local site didn’t work well on the background of heterozygous mutation of MEFV gene, thus, being triggered by mechanical operation of urinary tract, proliferation of nephrogenic adenoma was induced. However, an accumulation of the similar cases is mandatory to clearly elucidate the mechanisms of the disease. Furthermore, we should be aware that nephrogenic adenoma can occur in FMF patients to render a correct diagnosis.
Written informed consent was obtained from the patient’s father for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
We thank Mr. Masayuki Nagasaki and Ms. Mayuko Uegaki who provided superior technical assistance in immunohistochemistry and Ms. Hiroko Wada who assisted in molecular biology experiments.
- Kunji LP. Nephrogenic adenoma: report of a case and review of morphologic mimics. Arch Pathol Lab Med. 2010;134:1455–9.Google Scholar
- Davis TA. Hamartoma of the urinary bladder. Northwest Med. 1949;48:182–5.PubMedGoogle Scholar
- Mazal PR, Schaufler R, Altenhuber-Muller R, et al. Derivation of nephrogenic adenomas from renal tubular cells in kidney-transplant recipients. N Eng J Med. 2002;34:653–9.View ArticleGoogle Scholar
- Kibar Y, Sümer F, Yildirim I, Gamsizkan M, Avci A, Dayanç M. Nephrogenic adenoma of the bladder in a girl with Turner's syndrome: an unusual association. Int J Urol. 2004;11:795–7.View ArticlePubMedGoogle Scholar
- Vemulakonda VM, Kopp RP, Sorensen MD, Grady RW. Recurrent nephrogenic adenoma in a 10-year-old boy with prune belly syndrome: a case presentation. Pediatr Surg Int. 2008;24:605–7.View ArticlePubMedGoogle Scholar
- Sathe PA, Ghodke RK, Kandalkar BM. Mulifocal nephrogenic adenoma- a mimicker of malignancy. Indian I Pedatr. 2012;79:1661–3.View ArticleGoogle Scholar
- Campobasso P, Fasoli L, Dante S. Sodium hyaluronate in treatment of diffuse nephrogenic adenoma of the bladder in a child. J Pediatr Urol. 2007;3:156–8.View ArticlePubMedGoogle Scholar
- Siegal S. Benign paroxysmal peritonitis. Ann Intern Med. 1945;23:1–21.View ArticleGoogle Scholar
- Heller H, Sohar E, Sherf L. Familial Mediterranean fever. AMA Arch Intern Med. 1958;102:50–71.View ArticlePubMedGoogle Scholar
- Booth DR, Gillmore JD, Lachmann HJ, et al. The genetic basis of autosomal dominant familial Mediterranean fever. QJM. 2009;93:217–21.View ArticleGoogle Scholar
- The international FMF consortium. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell. 1997;90:797–807.View ArticleGoogle Scholar
- French FMF consortium. A candidate gene for familial Mediterranean fever. Nat Genet. 1997;17:25–31.View ArticleGoogle Scholar
- Yilmaz E, Ozen S, Balci B, Duzova A, Topaloglu R, Besbas N, et al. Mutation frequency of familial Mediterranean fever and evidence for a high carrier rate in the Turkish population. Eur J Hum Genet. 2001;9:553–5.View ArticlePubMedGoogle Scholar
- Goldfinger SE. Colchicine for familial Mediterranean fever. N Engl J Med. 1972;287:1302.PubMedGoogle Scholar
- Bhagavan BS, Tiamson EM, Wenk RE, Berger BW, Hamamoto G, Eggleston JC. Nephrogenic adenoma of the urinary bladder and urethra. Hum Pathol. 1981;12:907–16.View ArticlePubMedGoogle Scholar
- Tong GX, Melamed J, Mansukhani M, Memeo L, Hernandez O, Deng FM, et al. PAX2: a reliable marker for nephrogenic adenoma. Mod Pathol. 2006;19:356–63.View ArticlePubMedGoogle Scholar
- Tong GX, Weeden EM, Hamele-Bena D, Huan Y, Unger P, Memeo L, et al. Expression of PAX8 in nephrogenic adenoma and clear cell adenocarcinoma of the lower urinary tract: evidence of related histogenesis? Am J Surg Pathol. 2008;32:1380–7.View ArticlePubMedGoogle Scholar
- Kao CS, Kum JB, Fan R, Grignon DJ, Eble JN, Idrees MT. Nephrogenic adenomas in pediatric patients: a morphologic and immunohistochemical study of 21 cases. Pediatr Dev Pathol. 2013;16:80–5.View ArticlePubMedGoogle Scholar
- Srinivasula SM, Poyet JL, Razmara M, Datta P, Zhang Z, Alnemri ES. The PYRIN-CARD protein ASC is an activating adaptor for caspase-1. J Biol Chem. 2002;277:21119–22.View ArticlePubMedGoogle Scholar
- Chae JJ, Wood G, Masters SL, Richard K, Park G, Smith BJ, et al. The B30.2 domain of pyrin, the familial Mediterranean fever protein, interacts directly with caspase-1 to modulate IL-1β production. PNAS. 2006;26:9982–7.View ArticleGoogle Scholar
- Tomiyama N, Higashiuesato Y, Oda T, Baba E, Harada M, Azuma M, et al. MEFV mutation analysis of familial Mediterranean fever in Japan. Clin Exp Rheumatol. 2008;26:13–7.PubMedGoogle Scholar
- Duşunsel R, Dursun I, Gündüz Z, Poyrazoğlu MH, Gürgöze MK, Dundar M. Genotype-phenotype correlation in children with familial Mediterranean fever in a Turkish population. Pediatr Int. 2008;50:208–12.View ArticlePubMedGoogle Scholar
- Zadeh N, Getzug T, Grody WW. Diagnosis and management of familial Mediterranean fever: Integrating medical genetics in a dedicated interdisciplinary clinic. Genetics in medicine. 2011;13:263–9.View ArticlePubMedGoogle Scholar
- Sugiura T, Kawaguchi Y, Fujikawa S, Hirano Y, Igarashi T, Kawamoto M, et al. Familial Mediterranean fever in three Japanese patients, and a comparison of the frequency of MEFV gene mutations in Japanese and Mediterranean populations. Mod Rheumatol. 2008;18:57–9.View ArticlePubMedGoogle Scholar
- Mansfield E, Chae JJ, Komarow HD, Brotz TM, Frucht DM, Aksentijevich I, et al. The familial Mediterranean fever protein, pyrin, associates with microtubules and colocalizes with actin filaments. Blood. 2001;98:851–9.View ArticlePubMedGoogle Scholar
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.