Non-Parasitic Chyluria: a Rare Experience
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The Treatment of Chyluria Secondary to Advanced Carcinoma of the Prostate
Prostate Cancer and Prostatic Diseases (2008) 11, 102–105 & 2008 Nature Publishing Group All rights reserved 1365-7852/08 $30.00 www.nature.com/pcan CASE REPORT The treatment of chyluria secondary to advanced carcinoma of the prostate SA Cluskey, A Myatt and MA Ferro Department of Urology, Huddersfield Royal Infirmary, Huddersfield, UK Chyluria has not been previously reported as being associated with carcinoma of the prostate. The most common cause is lymphatic filariasis, a parasitic disease. Non-parasitic chyluria is rare. We describe a case of chyluria associated with carcinoma of the prostate. We describe our successful management in this case and highlight how urologists may overcome problematic chyluria in patients with advanced carcinoma of the prostate. Prostate Cancer and Prostatic Diseases (2008) 11, 102–105; doi:10.1038/sj.pcan.4500994; published online 31 July 2007 Keywords: chyluria; androgen blockade; TURP Introduction 3-week history of back pain. He had not opened his bowels for 3 days but reported passage of flatus. He Chyluria occurs as a result of abnormal communication was referred to the acute surgical team for further in- between lymphatics and the urinary tract. It may be vestigation. associated with flank pain, fever, dysuria, haematuria At the time of admission, his symptoms included and chylous clot retention.1–3 Worldwide, the most general malaise, back pain and poor mobility. He was common cause is lymphatic filariasis, a mosquito-borne indeed bed bound. He reported no difficulty in passing parasitic disease endemic to tropical and subtropical urine, although he had been treated for a suspected areas. -
Chyluria in Pregnancy-A Decade of Experience in a Single Tertiary Care Hospital
Nephro Urol Mon. 2015 March; 7(2): e26309. DOI: 10.5812/numonthly.26309 Research Article Published online 2015 March 1. Chyluria in Pregnancy-A Decade of Experience in a Single Tertiary Care Hospital 1 1,* 1 1 2 Khalid Mahmood ; Ahsan Ahmad ; Kaushal Kumar ; Mahendra Singh ; Sangeeta Pankaj ; 2 Kalpana Singh 1Department of Urology, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India 2Department of Gynaecology, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India *Corresponding author : Ahsan Ahmad, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India. Tel: +91-9431457764, E-mail: [email protected] Received: ; Revised: ; Accepted: December 29, 2014 January 4, 2015 January 22, 2015 Background: Chyluria i.e. passage of chyle in urine, giving it milky appearance, is common in many parts of India but rare in west. Very few case of chyluria in pregnant female has been reported in literature. Persistence of this condition may have deleterious effects on health of child and mother. In the present study 43 cases of chyluria during pregnancy and their management seen over a period more than 10 years have been presented. Objectives: The study aims to present our experience of managing 43 cases with chyluria during pregnancy over a period of ten years from July 2003 to June 2014. Patients and Methods: Forty three pregnant patients with chyluria, who presented between July 2003 to June 2014 to the department of Urology, Indira Gandhi Institute of Medical Sciences, Patna were included. Patients underwent conservative management and/or sclerotherapy after evaluation. Follow-up of all patients was done by observation of urine color, routine examination of urine and test for post prandial chyle in urine up to 3 months after delivery. -
Indirect Evaluation of Estrogenic Activity Post Heterotopic Ovarian Autograft in Rats1
12 - ORIGINAL ARTICLE Transplantation Indirect evaluation of estrogenic activity post heterotopic ovarian autograft in rats1 Avaliação indireta da atividade estrogênica após transplante heterotópico de ovário em ratas Luciana Lamarão DamousI, Sônia Maria da SilvaII, Ricardo dos Santos SimõesIII, Célia Regina de Souza Bezerra SakanoIV, Manuel de Jesus SimõesV, Edna Frasson de Souza MonteroVI I Fellow PhD Degree, Surgery and Research Post-Graduate Program, UNIFESP, São Paulo, Brazil. II Fellow Master Degree, Surgery and Research Post-Graduate Program, UNIFESP, São Paulo, Brazil. III Assistant Doctor, Gynecological Division, São Paulo University, Brazil. IV MS, Citopathologist, Gynecological Division, UNIFESP, São Paulo, Brazil. V Full Professor, Histology and Structural Biology Division, Department of Morphology, UNIFESP, São Paulo, Brazil. VI PhD, Associate Professor, Operative Technique and Experimental Surgery Division, Department of Surgery, UNIFESP, São Paulo, Brazil ABSTRACT Purpose: To morphologically evaluate the estrogenic effect on the uterus and vagina of rats submitted to ovarian autografts. Methods: Twenty Wistar EPM-1 adult rats were bilaterally ovariectomized, followed by ovarian transplants in retroperitoneal regions. The animals were divided in four groups of five animals, according to the day of euthanasia: G4, G7, G14 and G21, corresponding to the 4th, 7th, 14th and 21st day after surgery, respectively. Vaginal smears were collected from the first day of surgery until euthanasia day. After that, the vagina and uterus were removed, fixed in 10% formaldehyde and submitted to histological analysis and stained with hematoxiline and eosine. Results: All animals showed estrous cycle changes during the experiment. In 4th day, the uterus showed low action of estrogen with small number of mitosis and eosinophils as well as poor development. -
Paravertebral Extraosseous Ewing's Sarcoma
Unilateral pulmonary agenesis with AM. Philadelphia, W.B. Sunders Com- esophageal atressia and distal pany, 1996, pp 1199. tracheoesophageal fistula Report of two 6. Herbst JJ. The esophagus In Nelson Text cases J Pediatr Surg 1989; 24: 1084-1086. Book of Pediatrics, 15th edn. Eds. Behrman RE, Khegman RM, Arvind AM. 4. Sarin YK. Esophageal atresia and Philadelphia, W.B. Sounders Company, tracheoesophageal fistula with right pul- 1996, pp 1052-1053. monary agenesis Indian Pediatr 1996; 33: 595-597. 7. Mackinlay GA. Neonatal surgery In: ForFar and Arneils Text Book of Pediatrics, 5. Stern R, Congenital anomalies. In: 4th edn. Eds. Campbell AGM, Nelson Text Book of Pediatrics, 15th edn. Mcintosh N. Edinburgh, Churchill Eds. Behrman RE, Kliegman RM, Arvin Livingstone, 1992, pp 1850-1852. Paravertebral Extraosseous have been extremely rare To the best of Ewing's Sarcoma our knowledge EES located in paraverte- bral area has not been reported in Indian T.P. Yadav literature We report one such case R.P.Singh V.K. Gupta Case Report N.K. Chaturvedi* C. Vittal Prasad+ A 12-year-old male child was admitted with the complaints of progressively in- creasing dull aching pain in the upper back Extra Osseous Ewing's Sarcoma (EES) and right shoulder, radiating to the right has been considered a distinct clinico- hand since last two months and progres- pathological entity despite its striking ul- sive weakness of his right upper limb since trastructural similarity to Ewing's Sarcoma last one month Around the same time he of Bone (ESB) and same translocation -
Microrna Expression Signature of Human Sarcomas
Oncogene (2008) 27, 2015–2026 & 2008 Nature Publishing Group All rights reserved 0950-9232/08 $30.00 www.nature.com/onc ORIGINAL ARTICLE MicroRNA expression signature of human sarcomas S Subramanian1, WO Lui1, CH Lee1,2, I Espinosa1, TO Nielsen2, MC Heinrich3, CL Corless4, AZFire 1,5 and M van de Rijn1 1Department of Pathology, Stanford University, Stanford, CA, USA; 2Genetic Pathology Evaluation Centre, University of British Columbia, Vancouver, Canada; 3Division of Hematology/Oncology, Oregon Health and Science University, Portland, OR, USA; 4Department of Pathology, Oregon Health and Science University, Portland, OR, USA and 5Department of Genetics, Stanford University, Stanford, CA, USA MicroRNAs (miRNAs) are B22 nucleotide-long noncod- exist to help distinguish sarcoma subtypes, yet the recent ing RNAs involvedin several biological processes includ- advent of targeted drug therapies—as in the case of ing development, differentiation and proliferation. Recent gastrointestinal stromal tumor (GIST) and dermatofi- studies suggest that knowledge of miRNA expression brosarcoma protuberans—makes accurate diagnosis patterns in cancer may have substantial value for diagnostic imperative (Weiss and Goldbum, 2001). andprognostic determinations as well as for eventual MicroRNAs (miRNAs) are short, processed, RNA therapeutic intervention. We performedcomprehensive molecules B22 nucleotides in length that can control gene analysis of miRNA expression profiles of 27 sarcomas, 5 function through mRNA degradation, translation inhibi- normal smooth muscle and2 normal skeletal muscle tissues tion or chromatin-based silencing mechanisms (Doench using microarray technology and/or small RNA cloning and Sharp, 2004). In humans, about 500 miRNAs approaches. The miRNA expression profiles are distinct have been discovered so far (miRBase, Release 9.1; among the tumor types as demonstrated by an unsupervised http://microRNA.sanger.ac.uk/sequences) (Griffiths- hierarchical clustering, andunique miRNA expression Jones et al., 2006). -
Rhabdomyosarcoma of the Oral Cavity: a Case Report
Published online: 2019-09-30 Rhabdomyosarcoma of the Oral Cavity: A Case Report Ozkan Miloglua Sare Sipal Altasb Mustafa Cemil Buyukkurtc Burak Erdemcid Oguzhan Altune ABSTRACT Rhabdomyosarcoma (RMS), a tumor of skeletal muscle origin, is the most common soft tissue sarcoma encountered in childhood and adolescence. The common sites of occurrence are the head and neck region, genitourinary tract, retroperitonium, and, to a lesser extent, the extremities. In the head and neck region, the most commonly affected sites are the orbit, paranasal sinuses, soft tissues of the cheek, and the neck. RMS is relatively uncommon in the oral cavity, and the involve- ment of the jaws is extremely rare. Here, we report a case of oral RMS in a 13-year-old child and describe the clinical, radiological, histopathological, and immunohistochemical findings. (Eur J Dent 2011;5:340-343) Key words: Mouth neoplasm; Oral pathology; Alveolar rhabdomyosarcoma; Radiotherapy; Che- motherapy. INTRODUCTION Rhabdomyosarcoma (RMS), which was first tissue neoplasm of skeletal muscle origin. It ac- described by Weber in 1854, is a malignant soft counts for 6% of all malignancies in children un- der 15 years of age.1 The most commonly affected a Department of Oral Diagnosis and Radiology, Faculty of areas are the head and neck region, genitourinary Dentistry, Ataturk University, Erzurum, Turkey. tract, retroperitonium, and, to a lesser extent, the b Department of Pathology, Faculty of Medicine, Ataturk extremities.2 The head and neck RMSs are ana- University, Erzurum, Turkey. c Department of Oral and Maxillofacial Surgery, Faculty tomically divided into 2 categories: parameningeal of Dentistry, Sifa University, Izmir, Turkey. -
A Study of Anatomical Variations in the Arteries Supplying Gut Derivatives
Indian Journal of Anatomy99 Original Article Volume 3 Number 2, April - June 2014 A Study of Anatomical Variations in the Arteries Supplying Gut Derivatives Deepa G.*, Shivakumar G.L.** Abstract Anatomical variations in the branching pattern and distribution of the arteries supplying gut derivatives is very important especially for surgeons undertaking surgeries in the abdominal region. Anatomical variations contribute to the misinterpretation and leads to major postoperative complications. The present study was carried out in 32 adult cadavers (5 females and 27 male cadavers) which were used during routine dissection for undergraduate medical students. The course and branches of all the ventral branches of aorta was traced. Any arterial variation was observed and recorded. Anatomical variations related to the trifurcation of coeliac trunk, origin of the inferior phrenic artery, origin of the left gastric artery, origin of the accessory hepatic artery and the origin of the accessory right colic artery were noted and documented. In two cases, left colic artery was absent and inferior mesenteric artery gave rise to 3-4 sigmoid branches. The present study highlights on the importance of arterial variations in the abdomen which should not be ignored. Hence, the accurate knowledge of such variations is important in carrying out surgical procedures in the abdomen safely and also in the interpretation of angiographic reports. Keywords: Arteries; Anatomic variation; Abdomen; Aorta; Cadaver. Introduction coeliac trunk.[2] Superior mesenteric artery -
“Chyluria” a Rare Isolated Manifestation of Filariasis Dr
DOI: 10.21276/sjams.2017.5.2.65 Scholars Journal of Applied Medical Sciences (SJAMS) ISSN 2320-6691 (Online) Sch. J. App. Med. Sci., 2017; 5(2E):632-634 ISSN 2347-954X (Print) ©Scholars Academic and Scientific Publisher (An International Publisher for Academic and Scientific Resources) www.saspublisher.com Case Report “Chyluria” A Rare Isolated Manifestation of Filariasis Dr. Tejaswini N1, Dr. Mrudul Ramachandran Nair2, Dr. Rekha N H3 1Post Graduate student, 2Post Graduate student, 3Associate Professor Department of General Medicine, Rajarajeswari Medical College and Hospital, Bangalore, Karnataka *Corresponding author Dr. Rekha N H Email: [email protected] Abstract: Chyluria is an uncommon condition characterized by passage of milky urine. Lymphatic filariasis is the most common cause of chyluria. Here we are reporting a case of chronic chyluria in an adult married female, diagnosed for filarial infection by W. bancrofti and treated medically with resolution of symptoms. Keywords: Chyluria, Filariasis, Wuchereria Bancrofti INTRODUCTION Urine routine revealed proteinuria +++ and on Chyluria is a rare clinical symptom due to microscopy there were no pus cells. Urine was negative passage of milky urine. Chyluria is a urological for AFB stain and urine culture did not show any manifestation of abnormal lymphatic system due to growth. Urinary triglyceride level was 400mg/dl and we retrograde or lateral flow of lymph from the lymphatics also observed clearance of milky white colour of urine of the kidney, ureter or bladder allowing chylous on adding equal amount of Ether and mixing vigorously material to be discharged into the urinary collecting (Figure 2). Midnight peripheral smear and DEC system. -
A Case Report of Chyluria with Proteinuria
2012 iMedPub Journals Vol. 3 No. 4:1 Our Site: http://www.imedpub.com/ ARCHIVES OF CLINICAL MICROBIOLOGY doi: 10.3823/255 Puranjay Saha1, Soma Sarkar1, Dipankar Sarkar2*, A Case Report Manideepa SenGupta1 of Chyluria with 1 Department of Microbiology, 2 Department of Critical-Care Correspondence: Medical College & Hospital, Medicine, Columbia-Asia Proteinuria - Filarial Kolkata, West-Bengal, India Hospital, Kolkata, [email protected] West-Bengal, India origin? An enigma * Dipankar Sarkar Department of Critical-Care Medicine, Columbia-Asia Hospital, Kolkata, West-Bengal, India Abstract Filarial infections are common in most tropical and subtropical regions of the world. We report a case of chyluria due to lymphourinary fistula in a filarial antigen negative case, the diagnosis of which was confirmed by the demonstration of microfilariae in urine as well as in peripheral blood only after diethyl carbamazine (DEC) provocation test. So In endemic areas, workup of filarial infection should be considered in a patient with chyluria even if the filarial antigen is non-reactive and microfilaria cannot be demonstrated initially. This article is available from: Keywords: Filaria, Chyluria, Filarial antigen www.acmicrob.com Introduction Filarial infections are common in most tropical and subtropical regions of the world. Numerically, the public health problem of lymphatic filariasis is greatest in India, China and Indone- sia [1]. Lymphatic filariasis is caused by Wuchereria bancrofti, Brugia malayi, or Brugia timori. The clinical manifestations are directly related to the occlusion of the lymphatic channels, thereby causing lymphangiectasia [2]. The most common pre- sentations of lymphatic filariasis are subclinical microfilaremia, acute adenolymphangitis, hydrocele ,and chronic lymphatic disease[3]. -
Retroperitoneal Extra Adrenal Paraganglioma)
International Journal of Science and Research (IJSR) ISSN: 2319-7064 ResearchGate Impact Factor (2018): 0.28 | SJIF (2018): 7.426 Mysterious Mass in the Retroperitonium Space: Case Report (Retroperitoneal Extra Adrenal Paraganglioma) Dr. Rakshith, Dr. Jagadeesha BVC, Dr. Mahesh Kariyappa Abstract: Extra- adrenal retroperitoneal paragangliomas are extremely rare neuroendocrine neoplasms with an incidence of 2-8 per million. They emanate from embryonic neural crest cells and are composed mainly of chromaffin cells located in the para- aortic sympathetic chain. It is a kind of pheochromocytoma which occurs on the outside of the adrenal gland. They synthesize, store and secrete catecholamines due to which they may present with symptoms of hypertension like headache, sweating and palpitation and non functional paraganglioma sometimes they may present with vague symptoms like pain abdomen and lump abdomen. Primary methods of pre-operative diagnosis include imaging techniques which also help in surgical planning and pre-operative preparation of the patient. We present a case of non- functional extra- adrenal retroperitoneal paraganglioma occurring in a 40-year-old male patient presenting with mass per abdomen. On Ultrasonongraphy, suspicion was towards a retroperitoneal mass of probable retroperitoneal cyst. CT is the investigation of choice. Surgical resection is main modality of treatment. Confirmation of the diagnosis is done histopathological examination and immunohistochemistry markers. Keywords: retoperitoneal tumor: CD- Cluster of differentiation: paraganglioma 1. Introduction consistency, non ballotable and non pulsatile. Bowel sounds and rectal examination were normal. Paragangliomas (also known as extra-adrenal pheochromocytomas) are rare tumors that arise from extra- Ultrasonography was diagnosed as the retroperitoneal mass adrenal chromaffin cells1. -
Ganglioneuroma Mimicking Wilms' Tumor
Journal of Scientific Research and Studies Vol. 3(6), pp. 115-118, June, 2016 ISSN 2375-8791 Copyright © 2016 Author(s) retain the copyright of this article http://www.modernrespub.org/jsrs/index.htm MRRRPPP Case Report Ganglioneuroma mimicking Wilms’ tumor: Pediatric case report Qazi Adil INAM 1* and Abdul MANAN 2 1Department of Urology, Nawaz Sharif Medical College, University of Gujrat, Pakistan. 2Department of Urology and Renal Transplant, Services Hospital/Services Institute of Medical sciences, Lahore, Pakistan. *Corresponding author. E-mail: [email protected] Accepted 22 June, 2016 Ganglioneuroma is the tumor of sympathetic nerve fibers arising from neural crest cells. It may be present anywhere in the body along the autonomic nerve cells. This is usually a non-cancerous tumor. Its age incidence is between the 10-40 years of age. Usually tumor is asymptomatic; symptoms depend upon the location of tumor. In chest and pelvis, it may give symptoms by compression effect. Also, in the abdomen, mass may be palpable; this may be an incidental finding by radiologist. Radiological investigations may not differentiate this condition from other solid masses; misdiagnosis is common. Furthermore, the diagnosis is made on the basis of histopathology. Literature also shows that ganglioneuroma is misdiagnosed mostly. Key words: Retroperitoneal mass, neural crest cells, autonomic nerve cells, incidentalomas. INTRODUCTION Ganglioneuroma is a rare entity which arises from and females with enlarged clitoris. The most important sympathetic nerve fibers. The commonest sites are differential diagnosis is with neuroblastoma in which mediastinum, retroperitoneum and adrenal medulla but it urinary adrenaline, dopamine and VMA are raised may arise anywhere in the body usually along autonomic whereas, ganglioneuroma is usually hormonally silent nerve cells (Erem et al., 2008). -
SNAPSHOT SNAPSHOT “Milky” Urine: a Case of Chyluria
SNAPSHOT SNAPSHOT “Milky” urine: a case of chyluria A 53-YEAR-OLD Asian man with type 2 diabetes mellitus presented to the Emergency Department with acute onset of 1: Oral fat tolerance test generalised muscle cramps. He reported a 2-month history of polydipsia, polyuria and passing “milky” urine with blood clots. He had travelled widely throughout subtropical Asia. On examination, he was normotensive, with no lymphaden- opathy, abdominal masses or oedema. Urinalysis showed marked proteinuria, glycosuria and haematuria.The Medical The Journal urine ofprotein Australia excretion ISSN: 0025-729X rate was 19 later confirmedJanuary to 2004 be 15.57180 2 89-89 g/24 h (reference interval [RI], 0.02– 0.15 g/24©The h). Medical Urine Journal triglyceride of Australia measurement 2004 www.mja.com.au and lipopro- tein Snapshotelectrophoresis confirmed the appearance of chylo- microns in the urine after an oral fat tolerance test (Box 1). Biochemical analysis of serum showed the following levels: sodium 121mmol/L (RI, 134–146mmol/L), potassium 4.6mmol/L (RI, 3.4–5.3mmol/L), creatinine 46µmol/L (RI, Urine of patient before a 75 g oral fat tolerance test (0 h) and at 60–105µmol/L), glucose 19.7mmol/L (RI, <5.5mmol/L), fer- serial time points (0.5, 1, 2, 3, 4, and 5 h) after the test. ritin 16 mg/L (RI, 30–620mg/L), 25-hydroxyvitamin D 11nmol/L (RI, >50 nmol/L), total cholesterol 5.2mmol/L (RI, <5.5mmol/L), and triglyceride 1.8mmol/L (RI, <1.8mmol/L). 2: Contrast lymphangiography The patient had marked hypoproteinaemia and hypoalbumin- aemia, with a total protein level of 39g/L (RI, 63–80g/L) and albumin level of 21g/L (RI, 35–50g/L), respectively.