scholarly journals Lipoma of the sigmoid colon

2013 ◽  
Vol 70 (3) ◽  
pp. 319-321 ◽  
Author(s):  
Matilda Djolai ◽  
Bojana Andrejic ◽  
Dejan Ivanov
Keyword(s):  
Adipose Tissue ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Sigmoid Colon ◽  
Human Body ◽  
Soft Tissues ◽  
Benign Tumor ◽  
Extensive Resection ◽  
One Year ◽  
Histological Confirmation

Introduction. Lipoma is a benign tumor of adipose tissue, the most common tumor of the human body soft tissues. As such, it can be found almost anywhere in the human body including the gastrointestinal system (incidence below 0.5%), but rarely in the sigmoid colon. Case report. This is a case report on symptomatic polyp of the sigmoid colon, which after one year, at control colonoscopy, caused suspicion to malignancy. Endoscopically diagnosed polipoid lesion was laparoscopically removed. The pathohistological diagnosis determined benign, submucosal, incapsulated lipoma of the sigmoid colon. Conclusion. Although lipomas of the gastrointestinal tract are rare, this case clearly indicates that we should not prematurely and without histological confirmation of malignancy do more extensive resection for a suspected malignancy.

scholarly journals Synchronous Endometrial and Ovarian Cancer With Sigmoid Colon Metastasis One Year After Primary Surgery: A Case Report

2015 ◽  
Vol 3 (4) ◽  
pp. 220-222
Author(s):  
Kadir Guzin ◽  
Burcin Karamustafaoglu Balci ◽  
Kemal Sandal ◽  
Ahmet Gocmen ◽  
Ozgur Ekinci ◽  
...  
Keyword(s):  
Ovarian Cancer ◽  
Case Report ◽  
Sigmoid Colon ◽  
Primary Surgery ◽  
One Year ◽  
Colon Metastasis

scholarly journals Human penile ossification: case report

2007 ◽  
Vol 125 (2) ◽  
pp. 124-125 ◽  
Author(s):  
Homero Oliveira de Arruda ◽  
Hudson de Lima ◽  
Valdemar Ortiz
Keyword(s):  
Case Report ◽  
Rare Condition ◽  
Penile Shaft ◽  
Palpable Mass ◽  
Slight Pain ◽  
History Of ◽  
One Year ◽  
Histological Confirmation ◽  
Metaplastic Bone ◽  
Firm Mass

CONTEXT: Ossification in the human penis is such a rare condition that only 34 histologically evident cases have previously been reported. Among several conditions that have been correlated with this problem the most frequent is Peyronie disease. In all these conditions, human penile ossification appears to be a metaplastic bone formation process. CASE REPORT: A 59-year-old white man presented with a one-year history of slight pain upon erection and during intercourse. He also complained of hard plaque near the base of the penis. One year earlier, he had sustained blunt trauma during intercourse. Examination of the penis revealed a fixed firm mass extending over the proximal third of the penile shaft, measuring 3.0 x 3.0 x 2.0 cm and involving the corporal sponge, without surface extension. There was no impotence or other relevant clinical finding. Radiography on the penis revealed irregular calcification in the same position as the palpable mass and in the septum of the proximal inner third of the penis. The importance of this report lies in the extent of the human penile ossification, as demonstrated by the radiological and histological confirmation.

scholarly journals Plemorphic Adenoma of the Infratemporal Space: A New Case Report

2009 ◽  
Vol 2009 ◽  
pp. 1-3 ◽  
Author(s):  
Tarik El-Hadi ◽  
A. Oujilal ◽  
M. Boulaich ◽  
L. Sqalli ◽  
M. Kzadri
Keyword(s):  
Case Report ◽  
Salivary Glands ◽  
Pleomorphic Adenoma ◽  
Rare Case ◽  
Benign Tumor ◽  
Final Diagnosis ◽  
Complete Resection ◽  
Clinical Behaviour ◽  
Temporal Space ◽  
Histological Confirmation

Plemorphic adenoma is a frequent benign tumor of the major salivary glands. It could also develop from accessory salivary glands. We are reporting an extremely rare case of pleomorphic adenoma developing from the infratemporal space. The final diagnosis was based on histological confirmation. The treatment was mainly a complete resection via an anterior transmaxillary approach. Diagnosis, clinical behaviour, and treatment of pleomorphic adenoma of the infra-temporal space are reviewed from the literature.

scholarly journals Combined surgical and medical management for recurrent cellular angiofibroma of vulva in a young female - a case report

2016 ◽  
Vol 2 (1) ◽  
pp. 25
Author(s):  
Sasmita Das ◽  
Manisha Sahu ◽  
Amit K. Adhya ◽  
Ranjan K. Sahoo
Keyword(s):  
Adipose Tissue ◽  
Case Report ◽  
Genital Tract ◽  
Benign Tumor ◽  
Young Female ◽  
Gnrh Analogue ◽  
Male Genital Tract ◽  
Cellular Angiofibroma ◽  
Spindle Cells ◽  
Male Genital

<p class="abstract"><span lang="EN-US">Cellular angiofibroma of the vulva is a benign tumor of mesenchymal origin in female and male genital tract composed of stromal spindle cells and mixture of adipose tissue, prominently vascular in nature. Here we present a case of recurrent cellular angiofibroma in a 27 years old young woman which was the 5th time recurrence when she presented to us. Diagnosis was confirmed by MRI, histopathology study and immunohistochemistry. With wide excision of tumor followed by GnRH analogue therapy post operatively, she is now tumour free even after 20 months of surgery.</span></p>

scholarly journals Fibrous Hamartoma of Infancy in the Scrotum

2019 ◽  
Vol 07 (01) ◽  
pp. e100-e103
Author(s):  
Hrvoje Stepančec ◽  
Zoran Kokot ◽  
Draženko Keretić ◽  
Sandra Radiković ◽  
Donat Grgurović
Keyword(s):  
Case Report ◽  
Clinical Picture ◽  
Benign Tumor ◽  
Male Infant ◽  
Histopathological Analysis ◽  
Rare Tumor ◽  
Diagnostic Challenge ◽  
Fibrous Hamartoma Of Infancy ◽  
One Year

AbstractFibrous hamartoma of infancy is a solid benign tumor of the subcutis, which usually occurs within the first 2 years of life. It predominantly occurs in males, and is clinically presented as a solid, painless, well-limited subcutaneous formation, tending to grow, and in most cases without any symptoms. It occurs in various locations. The aim of this case report was to present a case of a rare tumor of infancy in the scrotal region, in an 8-month-old male infant, with a nonspecific clinical picture, suggestive of a malignant formation, thus presenting a diagnostic challenge for a doctor. The tumor was completely removed. The diagnosis was confirmed by histopathological analysis. One year after the surgical procedure, a follow-up ultrasonography examination showed no relapse.

Gastric choristoma of hypopharynx in neonate

2021 ◽  
Vol 70 (3) ◽  
pp. 174-176
Author(s):  
Kristýna Vaněčková ◽  
Zuzana Prouzová ◽  
Michal Jurovčík ◽  
Lucie Gernertová ◽  
Jiří Skřivan
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Gastric Mucosa ◽  
Benign Tumor ◽  
Orotracheal Intubation ◽  
Postnatal Period ◽  
Normal Cells ◽  
Difficulty Breathing ◽  
Specific Localization ◽  
Experienced Difficulty

Summary Gastric choristoma is composed of the ectopic microscopically normal cells of gastric mucosa and can be located anywhere in the gastrointestinal tract. Choristomas are mostly clinically silent or present with minimal symptoms and are usually dia­gnosed in adulthood. This case report presents a neonate who experienced difficulty breathing, dyspnea, orotracheal intubation and an early surgery in the postnatal period due to a specific localization and size of its tumor. Key words gastric choristoma – benign tumor – heterotophy – neonate

scholarly journals Follicular variant of ameloblastoma mandible reconstructed with free fibula: a case report

2017 ◽  
Vol 5 (1) ◽  
pp. 346
Author(s):  
Ramandeep Kaur ◽  
Vipin Arora ◽  
Sonal Sharma
Keyword(s):  
Case Report ◽  
Soft Tissues ◽  
Benign Tumor ◽  
Follicular Variant ◽  
Dental Lamina ◽  
Facial Disfigurement ◽  
Aesthetic Appearance ◽  
Odontogenic Epithelium ◽  
Free Fibula ◽  
Fibular Flap

Ameloblastoma is a tumor of odontogenic epithelium arising from remnants of dental lamina. It is a benign tumor but locally invasive affecting mandible more than maxilla. Ameloblastomas grow into the bone and soft tissues causing facial disfigurement and facial deformities. Treatment is surgical. We present a case report of 60 year old male with swelling in jaw, biopsy revealed ameloblastoma. Anterior segmental mandibulectomy was done and reconstructed with fibular flap which restored both function and aesthetic appearance.

scholarly journals Lipomatous polyp causing colo-colic intussusception

2020 ◽  
Vol 6 (7) ◽  
pp. 274
Author(s):  
Berhanetsehay Teklewold ◽  
Yisihak Suga ◽  
Tena Mamo ◽  
Mekete Wondewosen
Keyword(s):  
Adipose Tissue ◽  
Abdominal Pain ◽  
Gastrointestinal Tract ◽  
Soft Tissue ◽  
Ct Scan ◽  
Male Patient ◽  
Human Body ◽  
Soft Tissue Tumour ◽  
Tissue Tumour ◽  
Crampy Abdominal Pain

<p>A lipoma is a benign tumour that arises from an adipose tissue. It is the leading benign soft tissue tumour. It can occur anywhere in the human body. Lipomas in the gastrointestinal tract are quite rare and usually asymptomatic. We report a 70 years old male patient who presented with crampy abdominal pain. CT scan of the abdomen showed colo-colic intussusception. The patient was explored and the finding was colo-colic intussusception with a mass as a leading point. En-block resection done. Histology confirmed the mass as a lipoma.</p>

scholarly journals Pseudotumoral Calcinosis: A Soft Tissue Tumor in a 14-Year-Old Male

2020 ◽  
pp. 1-3
Author(s):  
Abderr Rahim ◽  
Abdelouahed Amrani ◽  
Abderr Rahim ◽  
Badr Rouijel ◽  
Imane Zizi ◽  
...  
Keyword(s):  
Soft Tissue Tumor ◽  
Soft Tissues ◽  
Benign Tumor ◽  
Tumoral Calcinosis ◽  
Calcium Deposition ◽  
Rare Benign Tumor ◽  
Hyperphosphatemic Familial Tumoral Calcinosis ◽  
One Year ◽  
The Right

Pseudotumoral calcinosis is a rare benign tumor, characterized by deep calcium deposition in peri-articular soft tissues. A numerous list of calcium deposit diseases exists making the calcinosis diagnosis very challenging. There are three principal forms or etiologies; primary or idiopathic forms followed by secondary forms due to chronic renal failure or hyperparathyroidism, then genetic forms such as Hyperphosphatemic Familial Tumoral Calcinosis (HFTC). We report a case of 14-year-old boy with primary tumoral calcinosis of the right hip. Total mass resection was performed without any recurrence at one-year follow-up.

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