Primary Duodenal Carcinoma - Case Report

2015 ◽  
Vol 86 (11) ◽  
Author(s):  
Mariusz Wesecki ◽  
Szymon Niemiec ◽  
Dagmara Radziuk ◽  
Dariusz Waniczek ◽  
Zbigniew Lorenc
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Female Patient ◽  
Surgical Intervention ◽  
Radical Surgery ◽  
Gastrointestinal Anastomosis ◽  
Advanced Stage ◽  
Rare Tumor ◽  
Staged Surgery ◽  
Duodenal Carcinoma

AbstractDuodenal carcinoma is a rare tumor of the gastrointestinal tract of an insidious and secretive course, often diagnosed during the advanced stage of the disease. The study presented a case of a female patient diagnosed with duodenal carcinoma, subjected to two-staged surgery. The initial surgical intervention consisted in the implementation of a gastrointestinal anastomosis, followed by radical surgery by means of Whipple's method performed after three years.

scholarly journals Isolated Duodenal Crohn's Disease: A Case Report and a Review of the Surgical Management

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Faruk Karateke ◽  
Ebru Menekşe ◽  
Koray Das ◽  
Sefa Ozyazici ◽  
Pelin Demirtürk
Keyword(s):  
Crohn’S Disease ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Crohn's Disease ◽  
Medical Treatment ◽  
Immunosuppressive Therapy ◽  
Surgical Management ◽  
Surgical Intervention ◽  
Surgical Options ◽  
Crohn’S Diseases

Crohn's disease may affect any segment of the gastrointestinal tract; however, isolated duodenal involvement is rather rare. It still remains a complex clinical entity with a controversial management of the disease. Initially, patients with duodenal Crohn' s disease (DCD) are managed with a combination of antiacid and immunosuppressive therapy. However, medical treatment fails in the majority of DCD patients, and surgical intervention is required in case of complicated disease. Options for surgical management of complicated DCD include bypass, resection, or stricturoplasty procedures. In this paper, we reported a 33-year-old male patient, who was diagnosed with isolated duodenal Crohn’s diseases, and reviewed the surgical options in the literature.

Mucocele of appendix: a case report

2021 ◽  
pp. 1-7
Author(s):  
Fareeha Farooqui ◽  
Sehrish Latif ◽  
Humera Naz Altaf ◽  
Sania Waseem ◽  
Sohaib Khan ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Surgical Management ◽  
Iliac Fossa ◽  
Mucinous Cystadenoma ◽  
Right Hemicolectomy ◽  
Unusual Presentation ◽  
Rare Tumor ◽  
Malignant Changes

Abstract Mucinous cystadenoma is a rare tumor of appendix it accounts for only 0.4% of the gastrointestinal tract malignancies and is reported rarely in literature. Therefore the surgical management is not yet established. Here we report a case of a 65 year old female who presented with a dragging sensation and a feeling of mass in right iliac fossa. Her computed tomography (CT) suggested an abscess formation of the parietal peritoneum. She was planned for laparotomy and upon exploration a mass was found arising from tip of retroperitoneal appendix. Whole of the appendix was studded with mucoid material. Limited right hemicolectomy was performed and histopathology of appendix showed mucinous cystadenoma with no evidence of malignant changes. Patient remained uneventful and was discharged on 4th post operative day. The unusual presentation of retroperitoneal pseudomyxoma without any intraperitoneal pathology, prompted us to report this case. Continuous...

scholarly journals Mandibular neurofibroma: Case report of a rare tumor

2019 ◽  
Vol 9 (4) ◽  
Author(s):  
Ziad Sleiman ◽  
Loubna Abboud ◽  
Elie Mehanna ◽  
Ramzi Mahmoud ◽  
Elie Yaacoub ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Surgical Management ◽  
Rare Tumor ◽  
Review Of The Literature ◽  
Histological Features ◽  
Jaw Bone

Neural tumors localized in jaw bone are relatively rare. This article presents a case of intraosseous neurofibroma of the mandible in a 37-year-old female patient. A review of clinical, radiographic, histological features and surgical management of the patient are discussed along with a review of the literature.

Renal Lipoma: a case report

Open Medicine ◽  
2013 ◽  
Vol 8 (3) ◽  
pp. 328-330
Author(s):  
Filip Vukmirović ◽  
Mihailo Vukmirović ◽  
Irena Vukmirović ◽  
Petar Kavarić
Keyword(s):  
Adipose Tissue ◽  
Case Report ◽  
Female Patient ◽  
Tumor Size ◽  
Single Case ◽  
Kidney Tissue ◽  
Rare Tumor ◽  
Mature Adipose Tissue

AbstractRenal lipoma is a very rare tumor that has only been described in about twenty cases in adults and in a single case in a child aged 2 years. This paper presents a renal lipoma in 63 year old female patient. The tumor size of 7.5×4.5 cm was located in her right kidney, clearly delineated from the surrounding kidney tissue, and histology was completely built of mature adipose tissue. This paper describes the case of a rare benign lipoma which histogenesis is yet not clearly understood.

scholarly journals A case of primary gastric melanoma

2020 ◽  
Vol 10 (1) ◽  
pp. 35-40 ◽  
Author(s):  
E. A. Toneev ◽  
A. L. Charyshkin ◽  
N. V. Dengina ◽  
A. V. Zhinov ◽  
A. A. Martynov ◽  
...  
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Rare Disease ◽  
Female Patient ◽  
Clinical Oncology ◽  
Skin Tumor ◽  
Upper Gastrointestinal Tract ◽  
Healthcare Institution ◽  
Complex Therapy ◽  
Upper Gastrointestinal

Primary gastric melanoma is an extremely rare disease. Melanoma of upper gastrointestinal tract usually occurs as metastasis from a primary skin tumor in 1 to 4 % of cases. The paper describes a case report of primary gastric melanoma in a female patient who received complex therapy at the State Healthcare Institution Ulyanovsk Regional Clinical Oncology Dispensary.

scholarly journals Effect of Unani formulations on frostbite induced gangrene: a case report

2020 ◽  
Vol 6 (3) ◽  
pp. 427
Author(s):  
Mohammad Shamim Khan
Keyword(s):  
Case Report ◽  
Oral Administration ◽  
Female Patient ◽  
Topical Application ◽  
Surgical Intervention ◽  
Surgery Patient

<p>This article reports a case in which a 65 years old female patient of frostbite induced gangrene, was treated with unani drugs; Sharbat Banafsha and Arq Murakkab Musaffi Khoon as oral administration, and Marham Safed Kafoori as topical application, with the aim to evaluate the efficacy of drugs and to avoid Surgery. Patient has shown excellent and admirable result within 60 days of treatment. Finally frost bitten and gangrenous part completely healed and repaired without any surgical intervention.</p>

scholarly journals Tulžies pūslės apsisukimas

2006 ◽  
Vol 4 (4) ◽  
pp. 0-0
Author(s):  
Kazys Katilius ◽  
Tomas Vaitoška ◽  
Agnė Vaitoškaitė
Keyword(s):  
Case Report ◽  
Bile Duct ◽  
Key Words ◽  
Female Patient ◽  
Surgical Intervention ◽  
Gallbladder Wall ◽  
Operative Intervention ◽  
Surgical Pathology ◽  
Postoperative Course ◽  
Emergency Hospital

Kazys Katilius, Tomas Vaitoška, Agnė VaitoškaitėVilniaus greitosios pagalbos universitetinė ligoninė, Šiltnamių g. 29, LT-04130 VilniusEl paštas: [email protected] Įvadas Pateikiama reta chirurginė patologija – tulžies pūslės gangrena dėl jos apsisukimo. Klinikinis atvejis Pacientė buvo hospitalizuota įtarus ūminį apendicitą. Diagnozė buvo neaiški, todėl ligonė stebėta. Vystantis peritonitui ligonė operuota. Atlikta vidurinė viršutinė laparotomija. Operacijos metu rasta apsisukusi ant pasaitėlio tulžies pūslė, turinti gangrenos požymių. Tulžies pūslės latakas nepakitęs. Tulžies pūslė pašalinta, jos pasaitėlis susiūtas, drenuotas dešinysis pašonkaulis. Laikotarpis po operacijos buvo sklandus. Atlikus pašalintos tulžies pūslės patologinį histologinį tyrimą, nustatytas tulžies pūslės sienos kraujotakos sutrikimas. Išvada Nepaisant sunkiai diagnozuojamos ir retai pasitaikančios ligos, ryžtingas ir laiku pasirinktas operacinis gydymas padėjo ligonei sėkmingai išgyti. Reikšminiai žodžiai: tulžies pūslės apsisukimas, cholecistektomija Gallbladder volvulus Kazys Katilius, Tomas Vaitoška, Agnė Vaitoškaitė.Vilnius University Emergency Hospital, Šiltnamių 29, LT-04130 Vilnius, LithuaniaE-mail: [email protected] Background A case report presents a patient with a rare surgical pathology – gallbladder volvulus. Case report A female patient presented at the hospital under suspicion of appendicitis. Because of undefined diagnosis the patient was examined. The progress of peritonitis determined her preoperational preparation and surgical intervention. The gallbladder twisted around its axis and gangrened was found during the procedure. The bile duct was found unaltered. Cholecystectomy was performed and the gallbladder pedicle was stitched and the subhepatic gap drenated. The postoperative course was uneventful. Pathistological examination showed acute hemorrhagic infarct in the gallbladder wall. Conclusion Despite an uncommon pathology hard for diagnoses, timely operative intervention provided for the convalescence of the patient. Key words: gallbladder volvulus, cholecystectomy

INTERDISCIPLINARY APPROACH FOR THE MANAGEMENT OF BILATERALLY IMPACTED MAXILLARY CANINES

2021 ◽  
pp. 80-82
Author(s):  
Kasturi Mukherjee ◽  
Amit Shaw ◽  
Manas Banerjee ◽  
Alangkar Saha
Keyword(s):  
Case Report ◽  
Treatment Planning ◽  
Female Patient ◽  
Patient Management ◽  
Surgical Intervention ◽  
Treatment Protocol ◽  
Interdisciplinary Approach ◽  
Holistic Approach ◽  
Adolescent Female ◽  
Treatment Goals

Interdisciplinary approach for the management of malocclusion provides a holistic approach of patient management. Prudent treatment planning is necessary to achieve the various treatment goals. This case report describes the orthodontic management of a 14-year-old adolescent female patient with bilateral labially impacted maxillary canines. The problems associated with impacted maxillary canines and the biomechanical interventions used for this patient are discussed. The treatment protocol involved surgical intervention, followed by sequential traction of the impacted teeth. An interdisciplinary approach to treatment with different mechanical strategies led to the achievement of the desired esthetic, functional, and occlusal treatment goals.

Primary Squamous Cell Carcinoma of the Stomach a Case Report

2005 ◽  
Vol 91 (5) ◽  
pp. 440-442 ◽  
Author(s):  
Yesim Yildirim ◽  
Zafer Akcali ◽  
Banu Bilezikci ◽  
Ozgur Ozyilkan
Keyword(s):  
Squamous Cell Carcinoma ◽  
Case Report ◽  
Cell Carcinoma ◽  
Squamous Cell ◽  
Advanced Stage ◽  
Rare Tumor ◽  
Rare Entity ◽  
Primary Squamous Cell Carcinoma ◽  
Carcinoma Of The Stomach

Squamous cell carcinoma (SCC) originating from the stomach is a relatively rare entity. There are theories regarding the development of this rare tumor, but its exact pathogenesis remains obscure. Fewer than 100 cases of primary SCC of the stomach have been presented in the literature. Due to the advanced stage at the time of diagnosis in most of these cases, the prognosis is generally poor. In the case presented here, dissemination of the tumor to the transverse colon, gallbladder and omentum was present at diagnosis. Despite the tumor's advanced stage, complete remission was achieved after six courses of adjuvant chemotherapy with 5-flourouracil and cisplatin. No recurrence has been detected during follow-up. The patient has been healthy with no sign of the disease for three years.

scholarly journals Successful Treatment of Hemorrhagic Bullous Henoch-Schönlein Purpura with Oral Corticosteroid: A Case Report

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Celebi Kocaoglu ◽  
Ramazan Ozturk ◽  
Yasar Unlu ◽  
Fatma Tuncez Akyurek ◽  
Sukru Arslan
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Female Patient ◽  
Oral Corticosteroid ◽  
Systemic Vasculitis ◽  
Immunoglobulin A ◽  
Henoch Schonlein Purpura ◽  
Hemorrhagic Bullae ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

Henoch-Schönlein purpura (HSP) is a vasculitis of small-sized blood vessels, resulting from immunoglobulin-A-mediated inflammation. It is the most common acute systemic vasculitis in childhood and mainly affects skin, gastrointestinal tract, joints, and kidneys. The characteristic rash of HSP consists of palpable purpuric lesions 2 to 10 mm in diameter concentrating in the buttocks and lower extremities. The occurrence of hemorrhagic bullae in children with HSP is rarely encountered. This report describes a 4.5-year-old female patient with HSP associated with hemorrhagic bullous lesions.

Sign in / Sign up

Export Citation Format

Share Document