Intraoral lipoma, surgical approach: A Case report

2020 ◽  
Author(s):  
Farnoosh Razmara ◽  
Nima Dehghani ◽  
Xaniar Mahmoudi ◽  
Mohammad Reza Reshadi ◽  
Mahdi Mohammadi
Keyword(s):  
Adipose Tissue ◽  
Buccal Mucosa ◽  
Benign Tumor ◽  
Surgical Techniques ◽  
Surgical Excision ◽  
Occurrence Rate ◽  
Common Region ◽  
Case Presentation ◽  
Rare Benign Tumor ◽  
Male Patients

Background: Lipoma is a rare benign tumor that overgrows in oral cavity. Its occurrence rate is about 1-4% with predilection for males rather than females. Lipoma is associated with adipose tissue and is usually seen in major salivary glands, buccal mucosa, and vestibule. Fifty percent of lesions are seen in buccal mucosa. The progressive and aggressive growth of these lesions may interfere with speech and mastication owing to the dimensions and location of the tumor. The lesion basically affects the individuals of 4th to 5th decades. Lipoma is managed by surgical excision using scalpel, laser, or electro-cautery. Case Presentation: This study presents two 63 and 18 years old male patients with lipoma in their buccal mucosa along with their improved situation following the treatment. The treatment included surgical excision of the lesion and suturing the surgical area. Conclusions: The incidence of intraoral lipoma is low and buccal mucosa is the most common region for the occurrence of oral lipoma. Most clinicians suggested surgical techniques as a certain treatment.

Eccrine Syringofibroadenoma of the Heel

2016 ◽  
Vol 106 (1) ◽  
pp. 76-78
Author(s):  
Nathalia Doobay ◽  
Jason Mallette
Keyword(s):  
Benign Tumor ◽  
Surgical Excision ◽  
Foot Pain ◽  
Rare Benign Tumor ◽  
Ductal Differentiation

Eccrine syringofibroadenoma is a rare, benign tumor of eccrine ductal differentiation, typically presenting in the extremities. Herein we report a case of a 77-year-old man with pain in the lateral midfoot and the presence of an eccrine syringofibroadenoma lesion in the lateral heel. On surgical excision of the lesion, the foot pain promptly resolved, and at the most recent follow-up visit, the patient remained pain free.

Tissue Maturation Correlating to Clinical Manifestations in Juvenile Angiofibroma

2005 ◽  
Vol 114 (9) ◽  
pp. 705-708 ◽  
Author(s):  
Luiz U. Sennes ◽  
Felipe S. G. Fortes ◽  
Ossamu Butugan ◽  
Paulo H. Saldiva ◽  
Fabiola C. Bernardi
Keyword(s):  
Nasal Obstruction ◽  
Benign Tumor ◽  
Clinical Manifestations ◽  
Young Male ◽  
Previous Treatment ◽  
Facial Deformity ◽  
Nasopharyngeal Angiofibroma ◽  
Tumor Number ◽  
Rare Benign Tumor ◽  
Male Patients

Objectives: Juvenile nasopharyngeal angiofibroma is a rare benign tumor that affects young male patients and shows a characteristic development from its origin. It is not a true neoplasm, but shows features of vascular processes, developing into a more fibrous condition. The aim of this study was to correlate the clinical manifestations and the histologic findings of the tumor. Methods: Thirty-six patients without previous treatment were studied. We correlated the incidence and duration of the clinical manifestations (nasal obstruction, epistaxis, nasal and/or pharyngeal tumor, and facial deformity) and morphometric histologic analyses of the central region of the tumor (number, caliber, and presence of muscle cells in the vessel wall, and tissue maturity and cellularity). Results: The duration of nasal obstruction, the presence of nasal and/or pharyngeal tumor, and facial deformity were significantly correlated with the number of vessels, the tissue maturation, and the cellularity of the tumor. Epistaxis showed a strong correlation with the presence of muscle fibers in the vessels. Conclusions: There are correlations between the duration of the clinical manifestations and histologic maturation in the central portion of the tumor.

scholarly journals Voluminous Extracardiac Adult Rhabdomyoma of the Neck: A Case Presentation

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Riccardo Maglio ◽  
Scicchitano Francesco ◽  
Magistri Paolo ◽  
Valabrega Stefano ◽  
D'Angelo Francesco ◽  
...  
Keyword(s):  
Head And Neck ◽  
Benign Tumor ◽  
The Body ◽  
Differential Diagnoses ◽  
Mesenchymal Tumors ◽  
Adult Type ◽  
Case Presentation ◽  
Italian Patient ◽  
First Case ◽  
Rare Benign Tumor

Introduction. Rhabdomyomas of the head and neck are exceptionally rare benign mesenchymal tumors. Rare cases have been reported to involve other sites of the body including the head and neck regions.Case Presentation. We report a case of voluminous extracardiac adult rhabdomyoma affecting adult patients and initially seen as slowly growing, indolent neoplasms. The patient is a seventy-year old male Italian patient.Conclusion. Adult extracardiac rhabdomyoma is a rare benign tumor that may present with symptoms that vary from aerodigestive tract obstruction to remaining asymptomatic for many years. Although histology is very characteristic, several differential diagnoses have to be considered. To our knowledge, this is the first case of voluminous adult-type symptomless rhabdomyoma.

scholarly journals Spongiotic osteoma in the external auditory canal: Two cases of a rare tumor

2020 ◽  
Vol 8 ◽  
pp. 2050313X2098146
Author(s):  
Kyuin Lee ◽  
Yoon Jung Choi ◽  
Hyun Seung Choi ◽  
Junhui Jeong
Keyword(s):  
External Auditory Canal ◽  
Benign Tumor ◽  
Conductive Hearing Loss ◽  
Surgical Excision ◽  
Rare Tumor ◽  
Debris Accumulation ◽  
Rare Benign Tumor ◽  
Diamond Burr ◽  
Conductive Hearing ◽  
Histopathologic Findings

Osteoma of the external auditory canal is a rare benign tumor with an estimated incidence of 0.05% of total otologic surgeries. In most cases, an osteoma in the external auditory canal does not cause symptoms because the tumor grows slowly and does not occlude the ear canal. However, if the mass grows to occlude the external auditory canal, several symptoms can occur, including conductive hearing loss, aural fullness, and keratin debris accumulation. We present two cases of this rare tumor in a 23-year-old woman and a 19-year-old man. The mass was surgically excised at the level of the peduncle under local anesthesia with microscope assistance. The base of the excised mass was drilled with a diamond burr to remove all osseous lesions. Histopathologic findings showed spongiotic osteomas. In these cases, patients had symptoms of aural fullness, although the osteomas did not completely occlude the external auditory canal, and the symptoms improved after surgical excision without recurrence.

scholarly journals Large Brunner’s gland adenoma of the duodenum for almost 10 years

2020 ◽  
Vol 15 (1) ◽  
pp. 237-240
Author(s):  
Bo Yang ◽  
Ke Li ◽  
Runlan Luo ◽  
Zuming Xiong ◽  
Lianwei Wang ◽  
...  
Keyword(s):  
Benign Tumor ◽  
Accurate Diagnosis ◽  
Case Presentation ◽  
Brunner's Glands ◽  
Gastrointestinal Obstruction ◽  
Brunner’S Glands ◽  
Rare Benign Tumor ◽  
Brunner’S Gland ◽  
Brunner's Gland ◽  
Upper Gastrointestinal

AbstractBackgroundBrunner’s gland adenoma is a rare benign tumor arising from Brunner’s glands. It is mostly small in size, and patients with this tumor are asymptomatic.Case presentationWe report the case of a 63-year-old woman with upper gastrointestinal obstruction for almost 10 years, who was pathologically diagnosed with large Brunner’s gland adenoma of the duodenum. Postoperatively, no sign of recurrence has been noted until now.ConclusionThis study may help clinicians to understand and provide a more accurate diagnosis of Brunner’s gland adenoma.

scholarly journals Desmoplastic fibroma of the left 6th rib in a 35-year-old man: a case report and literature review

2021 ◽  
Author(s):  
Kai Zhang ◽  
Wu Weibin ◽  
Guan Jiexia ◽  
Wu Yonghui ◽  
Chen Huiguo ◽  
...  
Keyword(s):  
Local Recurrence ◽  
Benign Tumor ◽  
Surgical Excision ◽  
Final Diagnosis ◽  
High Rate ◽  
Wide Resection ◽  
Desmoplastic Fibroma ◽  
Left Chest ◽  
Rare Benign Tumor ◽  
Enhanced Computed Tomography

Abstract Background: Desmoplastic fibroma (DF) is a rare, benign tumor. The most common sites are the long tubular bones and mandible. Although generally considered a benign tumor, it can invade surrounding tissues and has a high rate of local recurrence after incomplete surgical excision. However, there is currently no stantard treatment. Here we present a novel case of DF in the left 6th rib in a 35-year-old man.Case presentation: The man presented to our center with left chest pain and swelling. Enhanced computed tomography (CT) showed a 4.5×2.0 cm mass on the left 6th rib with pathological fracture.Wide resection was performed. Open biopsy revealed that the tumor destroyed medullary cavity and partially broke through the bone cortex. Pathologically, the tumor was composed of spindle-shaped cells arranging in a woven pattern on a backgroung of abundant collagenous fiber. No β-catenin were detected. Based on the pathological and radiological findings, a final diagnosis of DF was made. No postoperative adjuvant treatments were administerded. Fortunately, there was no evidence of recurrence 22 months after surgery. Conclusions: DF originated from rib is a kind of extremly rare benign tumor but locally aggressive and show unique biologically features. Wide resection or total resection can effectively reduce the risk of local recurrence when compared with curettage. Rarity of the tumor favors documentation in literature.

scholarly journals A Misdiagnosis of a Huge Lung Fibroleiomyomatous Hamartoma in Pleural Cavity

2021 ◽  
Author(s):  
Minghui Liu ◽  
Xin Li ◽  
Hongbing Zhang ◽  
Fan Ren ◽  
Ming Dong ◽  
...  
Keyword(s):  
Benign Tumor ◽  
Pleural Cavity ◽  
Good Prognosis ◽  
Positive Staining ◽  
Case Presentation ◽  
Napsin A ◽  
Mediastinal Germ Cell Tumor ◽  
S 100 ◽  
Rare Benign Tumor ◽  
Percutaneous Lung Biopsy

Abstract Backgroud: Lung fibroleiomyomatous hamartoma is an extremely rare benign tumor in lung, it belongs to hamartoma. There were only five patients with solitary pulmonary fibroleiomyomatous hamartoma reported in literatures and our case has the largest size of the tumor from lung.Case presentation: Our case is a 36-year woman with a huge mass in pleural cavity. She was once misdiagnosed mediastinal germ cell tumor with pleural effusion through percutaneous lung biopsy in other hospital. After traditional thoracotomy, a huge size of 22 x 18 x 5.5 cm mass was completely dissected and a diagnosis of pulmonary fibroleiomyomatous hamartoma was given by pathology combined with immunohistochemical staining, which showed the positive staining of SMA, Desmin, CD34, BCL2, TTF1, Napsin A, and CK7, and the negative staining of S-100 and Calretinin. The patient recovered well with 40 months following up without recurrence.Conclusions:In our case, we had reported the largest size of lung fibroleiomyomatous hamartoma. The treatment of fibroleiomyomatous hamartoma is completely resected it and have a good prognosis.

scholarly journals Adult pancreatic cavernous hemangioma: case presentation of a benign tumor with a complex composition

2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Tao Lianyuan ◽  
Wang Yafeng ◽  
Yu Haibo ◽  
Dong Yadong ◽  
Ma Jiahao ◽  
...  
Keyword(s):  
Cavernous Hemangioma ◽  
Benign Tumor ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Complex Composition ◽  
Ki 67 ◽  
Case Presentation ◽  
Multilocular Cyst ◽  
Imaging Examination ◽  
Upper Abdominal

Abstract Background Pancreatic cavernous hemangioma is an extremely rare benign tumor that is difficult to diagnose on an imaging examination, and its histopathological examination has rarely been reported. Case presentation Herein, we present the case of a 63-year-old man who was admitted to the hospital due to left upper abdominal pain and defecation unformed for more than 2 years. None of the positive results obtained from the physical examination could explain his symptoms. The imaging examination indicated a multilocular cyst with septa in the head of the pancreas. The patient underwent a pancreaticoduodenectomy, and the pathologic diagnosis was pancreatic cavernous hemangioma. The histopathological examination showed that the lesion was positive for benign vascular markers, such as CD31, CD34 and F8, and negative for lymphocyte markers, such as D2–40. Moreover, it was also positive for ERG and cytokeratin markers, CAM5.2 and AE1/AE3, indicating the complexity of its components, and Ki-67 negativity revealed its benign nature. Conclusions Pancreatic cavernous hemangioma has a complex composition that may be reflected not only in the imaging examination but also in the immunohistochemical detection, and it may achieve a good outcome by surgical excision.

scholarly journals A Rare Benign Tumor in a 14-Year-Old Girl

2018 ◽  
Vol 2018 ◽  
pp. 1-4
Author(s):  
Meral Hassan Abualjadayel ◽  
Osama Y. Safdar ◽  
Maysaa Adnan Banjari ◽  
Sherif El Desoky ◽  
Ghadeer A. Mokhtar ◽  
...  
Keyword(s):  
Benign Tumor ◽  
Renal Oncocytoma ◽  
Pathology Report ◽  
Renal Neoplasm ◽  
Case Presentation ◽  
Renal Oncocytomas ◽  
Rare Benign Tumor ◽  
History Of ◽  
Tract Infections ◽  
Left Flank Pain

Background. Oncocytomas are the second most common benign renal neoplasm but, unfortunately, they are difficult to differentiate from renal cell carcinoma. Renal oncocytomas are rare and have mostly been reported in adults. To our knowledge, this is only the sixth pediatric reported case of renal oncocytoma worldwide. Case Presentation. A 14-year-old Yemeni girl with a recurrent history of urinary tract infections came to our clinic complaining of left flank pain with a frontal headache. Ultrasound showed a 3 cm, well-defined echogenic lesion with mild vascularity. This lesion increased in size on her subsequent follow-ups. Computed tomography showed no intralesional fat, vessels invasion, or enlarged lymph nodes. The patient underwent laparoscopic radical nephrectomy, and a pathology report confirmed the diagnosis of renal oncocytoma. Conclusion and Recommendations. We present the rare occurrence of renal oncocytoma in a pediatric patient and highlight the importance of considering oncocytomas in the diagnosis of a renal mass.

scholarly journals Retroperitoneal angioleiomyomatosis

2020 ◽  
Author(s):  
Luz Angela Torres-de la Roche ◽  
Rajesh Devassy ◽  
Ghaith Makhlouf ◽  
Johannes San Juan ◽  
Jennifer Eidswick ◽  
...  
Keyword(s):  
Benign Tumor ◽  
Surgical Techniques ◽  
Vascular Complications ◽  
Intravenous Leiomyomatosis ◽  
Significant Morbidity ◽  
Rare Benign Tumor

AbstractRetroperitoneal intravenous leiomyomatosis is a rare benign tumor that can spread through veins carrying significant morbidity. The challenge of its management lies within the complexity of completely excising the tumor, which if carried out improperly can result in neurological or vascular complications requiring complex reparative surgeries. Here we present the successful resection of a retroperitoneal angio-leiomyoma by combining laparoscopic route, micro-surgical techniques and modern endoscopic tools.

Sign in / Sign up

Export Citation Format

Share Document