Leiomyosarcome du Rein: A Propos D’un Cas

Le léiomyosarcome du rein est une tumeur rare. Les auteurs ont rapporté l’observation d’un homme âgé de 45 ans, chez lequel le diagnostic d’une tumeur rétropéritoénale gauche a été posé lors de l’exploration de douleurs du flanc gauche associées à une altération de l’état général et ce par l’imagerie (Echographie et scanner abdominal). La laparotomie exploratrice avait conclu à une tumeur rénale gauche localement évoluée, une néphrectomie élargie a été réalisée et l’histologie était en faveur d’un léiomyosarcome rénal. Une récidive locale a été diagnostiquée après un recul de 6 mois. Après une nouvelle laparotomie, l’abstention était de mise devant le caractère évolué de la récidive. Le but de cette observation est double. Le premier, est la nécessité de faire un diagnostic précoce, afin d’intervenir sur une tumeur de petite taille, plus accessible à la chirurgie. Le second, est de discuter la place du traitement adjuvant, qui pourrait réduire le risque de récidive précoce.Mots clés : Léiomyosarcome, rei

Primary Plasmacytoma of The Testis with no Evidence of Multiple Myeloma: a New Case Report and Literature Review

Plasmacytomas of the testis are extremely rare tumours, especially when occurring in the absence of a previous or concurrent diagnosis of multiple myeloma. We report a new case of solitary testicular plasmacytoma, with immunohistochemical studies showing monoclonal cytoplasmic production of IgG lambda light chains, in a 51-year-old man who had no evidence of multiple myeloma 3 years after the orchiectomy.Key Words: Testis, plasmacytoma, multiple myelom

Paratesticular Liposarcoma: What is the Best Therapeutic Strategy?

Introduction: Liposarcomas are neoplasms of mesodermal origin derived from adipose tissue and correspond to 10–14% of all soft tissue sarcomas. Paratesticular liposarcoma is very rare.Case report: We report a 60-year old man who presented with a left testicular tumor 20 cm in diameter. Initial incisional biopsy was reported as fibromatosis. Chest and abdominal CT scan did not show distant metastases. Through an inguinal incision orchidectomy with homolateral inguinal node dissection was performed. Histopathological examination showed a paratesticular myxoid liposarcoma. Adjuvant radiotherapy without chemotherapy was administered. The patient remains well at 11 months followup, with no evidence of recurrence.Conclusion: Complete surgical extirpation reduces the risk of local recurrence. Neoadjuvant chemotherapy or radiotherapy may reduce the tumor size, thus facilitating complete excision

Complications after intestinal resection in Crohn's disease: laparoscopic versus conventional approach

AbstractBackgroundsignificant advances in medical therapy for Crohn's disease (CD) occurred in the last 12 years, mainly due to the introduction of anti-TNF therapy. Laparoscopic colorectal surgery represented the most important advance on surgical treatment in the management of CD, as it also had developed in the treatment of other conditions. There is a tendency for lower complication rates after laparoscopic bowel resections as compared to open surgery. The aim of this study was to analyze and compare the complication rates after bowel resections for CD between the two approaches in a Brazilian case series.Methodsthis was a retrospective longitudinal study, including CD patients submitted to bowel resections from a single Brazilian Inflammatory Bowel Diseases (IBD) referral center, treated between January 2008 and June 2012 with laparoscopic approach (LA) or conventional approach (CA).Variables analyzedage at surgery, gender, Montreal classification, smoking, concomitant medication, type of surgery, surgical approach, presence and type of complication up to 30 days after the procedures. Readmission and reoperation rates, as well as mortality, were also analyzed. Patients were allocated in two groups regarding the type of procedure (LA or CA), and complication rates and characteristics were compared. Statistical analysis was performed with Mann-Whitney test (quantitative variables) and chi-square test (qualitative variables), with p < 0.05 considered significant.Resultsa total of 46 patients (25 men) were included (16 submitted to LA), with mean age of 38.1 (± 12.7) years. The groups were considered homogeneous according to age, gender, CD location, perianal disease and concomitant medications. There were more patients with fistulizing CD on the CA group (p = 0.029). The most common procedure performed was ileocolic resection on both groups (56.7% of the CA and 75% of the LA patients – p = 0.566). Overall, total complications (surgical and medical, including minor and major issues) oc- curred in 60% (18/30) of the CA group and 12.5% (2/16) of the LA group (p = 0.002). Wound in- fection was the most frequent complication (10/30 on CA and 1/16 on the LA groups). There were 3 deaths in the CA group. Specific analysis of each complication did not demonstrate any difference between the groups regarding abdominal sepsis, urinary tract infections, pneumonia, readmission, reoperations and deaths (p = 0.074).Conclusionsthere was a higher complication rate in patients operated with CA as compared to LA. This was probably due to patient selection for the laparoscopic approach, with severe cases, mostly due to fistulizing abdominal CD, being operated mainly by open surgery. LA tends to be the recommended approach in most cases of non-complicated CD

Tumeur maligne des gaines nerveuses périphériques révélant une neurofibromatose type 1

La Neurofibromatose type 1 (NF1) ou maladie de Von Recklinghausen est une affection à expression clinique variable. La transformation maligne est rare et redoutable. Le but de ce travail est d’étudier les critères diagnostiques ainsi que la prise en charge thérapeutique de cette transformation maligne. Observation : A.B, âgé de 16 ans, a consulté pour une tuméfaction basicervicale antérieure d’apparition récente, ayant augmenté progressivement de taille sans signes de compression ni de dysthyroïdie. L’examen clinique a trouvé une masse dure, bien limitée, indolore, de 4 cm de grand axe siégeant en regard du manubrium sternal, adhérente au plan profond et débordant sur le creux sus sternal. A cette masse s’associaient des taches cutanées café au lait disséminées sur tout le corps, des nodules de Lish iriens et des neurofibromes occipitaux et parotidiens. Après une exérèse de la masse par voie cervicale, l’examen histologique a conclu à une tumeur maligne de la gaine nerveuse. Le malade a eu dans un 2ème temps, une exérèse plus large emportant le manubrium sternal et les tissus adjacents  avec une reconstruction par des fragments de côtes mais avec des limites chirurgicales envahies. L’évolution a été marquée par une poursuite évolutive précoce imposant une exérèse chirurgicale plus large suivie d’une chimiothérapie et d’une radiothérapie externe (RT). Le malade était cependant toujours en poursuite évolutive et le décès est survenu dans un contexte d'envahissement médiastinal.Mots-clés : Neurofibromatose type 1, Sarcome, tissus mous, gaines nerveuses périphériques, Chirurgie