scholarly journals Mural ameloblastoma- A case report

2021 ◽  
Vol 7 (4) ◽  
pp. 302-305
Author(s):  
Sruthi Chandra V ◽  
V Ramesh ◽  
P D Balamurali ◽  
Nirima Oza
Keyword(s):  
Case Report ◽  
Benign Neoplasm ◽  
Risk Of Recurrence ◽  
Epithelial Origin

Ameloblastoma is a benign neoplasm of odontogenic epithelial origin which comprises of several clinical, radiological and histological varieties. Among these, unicystic variant is the least explored and its mural subtype shows a high aggressiveness and risk of recurrence and comparable with that of conventional ameloblastoma. Herein, we present a case of mural ameloblastoma of maxilla in a 32-year old female.

scholarly journals Giant retroperitoneal lipoma: a case report

2003 ◽  
Vol 40 (4) ◽  
pp. 251-255 ◽  
Author(s):  
Carlos Augusto Real Martinez ◽  
Rogério Tadeu Palma ◽  
Jaques Waisberg
Keyword(s):  
Case Report ◽  
Histological Study ◽  
Abdominal Mass ◽  
Benign Neoplasm ◽  
Large Mass ◽  
White Female ◽  
Ascending Colon ◽  
Abdominal Ultrasonography ◽  
History Of ◽  
History Of Pain

BACKGROUND: Retroperitoneal lipoma is an extremely rare neoplasm. AIMS: The authors report a case of giant retroperitoneal lipoma in a 32-year-old white female, with a history of pain and an abdominal mass over a 2-year period. Total abdominal ultrasonography and barium enema showed a large mass located in the retroperitoneal space behind the ascending colon. Laparotomy showed a large encapsulated tumor measuring 20 x 13 x 10 cm and weighing 3.400 g. The histological study revealed a benign neoplasm of fatty cells. CONCLUSION: The patient remains well 17 years after surgery, without recurrentce of the disease.

scholarly journals Laryngeal Amyloidosis: A Case Report

2020 ◽  
Vol 7 ◽  
Author(s):  
Mohamed Mouzouri ◽  
Adil Eabdenbitsen ◽  
Azeddine Lachkar ◽  
Mohamed Rachid Ghailan
Keyword(s):  
Case Report ◽  
Common Symptom ◽  
Vocal Cords ◽  
Risk Of Recurrence ◽  
Clinical Symptomatology ◽  
Systemic Dissemination ◽  
Laryngeal Amyloidosis ◽  
Localized Form

Introduction: laryngeal amyloidosis is an uncommon localized form of amyloidosis. The clinical symptomatology is not specific, and the diagnosis should be evoked in a persistent dysphonia.Case report: A 45-year-old patient who had consulted for dysphonia lasting for 2 years. The nasofibroscopy showed an infiltrative lesion of the vocal cords. The laryngeal biopsy was performed and revealed laryngeal amyloidosis. Search for other locations were negative.Conclusion: dysphonia is the most common symptom of laryngeal amyloidosis. Monitoring is extended because of the risk of recurrence and systemic dissemination.

scholarly journals Inflammatory Myofibroblastic Tumor of the Epiglottis Excised with a Carbon Dioxide Laser: Case Report and Literature Review

2018 ◽  
Vol 97 (8) ◽  
pp. E31-E33 ◽  
Author(s):  
Blake Raggio ◽  
Neil Chheda
Keyword(s):  
Carbon Dioxide ◽  
Case Report ◽  
Adjuvant Therapy ◽  
Literature Review ◽  
Carbon Dioxide Laser ◽  
Inflammatory Myofibroblastic Tumor ◽  
Benign Neoplasm ◽  
First Case ◽  
Laser Excision

Inflammatory myofibroblastic tumor (IMT) is a benign neoplasm of intermediate biologic potential. It rarely occurs in the larynx, and it has not been previously reported in the epiglottis. We treated a 66-year-old woman who presented with progressive dysphonia and a mass on her suprahyoid epiglottis. The tumor was completely excised with a CO2 laser; no adjuvant therapy was administered. Histopathology revealed that the mass was an IMT. No evidence of recurrence was noted after 6 months of follow-up. We present what we believe is the first case of an epiglottic IMT to be reported in the literature, and we propose CO2 laser excision without adjuvant therapy as an acceptable treatment.

scholarly journals Spindle Cell Hemangioendothelioma of the Temporal Muscle Resected with Zygomatic Osteotomy: A Case Report of an Unusual Intramuscular Lesion Mimicking Sarcoma

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Tomohiro Minagawa ◽  
Takeshi Yamao ◽  
Ryuta Shioya
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Soft Tissue ◽  
Soft Tissue Sarcoma ◽  
Spindle Cell ◽  
Neck Region ◽  
Benign Neoplasm ◽  
Low Grade ◽  
Temporal Muscle ◽  
Head And Neck Region

Spindle cell hemangioendothelioma (SCH) was originally described by Weiss and Enzinger (1986) as a low-grade angiosarcoma resembling both cavernous hemangioma and Kaposi's sarcoma. Recent studies suggest that SCH is a benign neoplasm or reactive lesion accompanying a congenital or acquired vascular malformation. Most SCHs present as one or more nodules affecting the dermis or subcutis of the distal extremities. Few reports describe SCH of the head and neck region; even fewer note intramuscular SCH. Here, we describe a case of SCH involving the temporal muscle mimicking soft tissue sarcoma, who had a successful surgical treatment with a coronal approach and zygomatic osteotomy.

scholarly journals Lipoma of the Palate: An Uncommon Finding

2016 ◽  
Vol 10 (1) ◽  
pp. 643-646 ◽  
Author(s):  
Luiz Evaristo Ricci Volpato ◽  
Artur Cunha Vasconcelos ◽  
Nayane Assis Lambert ◽  
Paulo Henrique de Souza Castro ◽  
Arlindo Aburad ◽  
...  
Keyword(s):  
Case Report ◽  
Hard Palate ◽  
Case Reports ◽  
Benign Neoplasm ◽  
Benign Tumors ◽  
Rare Entity ◽  
Local Inflammation ◽  
Total Resection ◽  
Endocrine Factors ◽  
Adipose Cells

Background: Lipoma is a benign neoplasm originated from adipose cells circumscribed by connective tissue. This neoplasm represents about 1% to 4.4% of all oral benign tumors and it is rarely located in the palate area. Objective: This case reports the occurrence of an oral lipoma in the hard palate of a 57-year-old woman and discusses its etiology and treatment. Case Report: The treatment consisted in the total resection of the lesion and laser therapy. The patient is being followed up for forty three months with no signs of recurrence. Conclusion: Lipoma in hard palate is a rare entity that may be associated with endocrine factors and local inflammation.

scholarly journals A Case Report of a Solitary Fibrous Tumor of the Maxillary Sinus

Reports ◽  
2021 ◽  
Vol 4 (4) ◽  
pp. 33
Author(s):  
Mattia Di Bartolomeo ◽  
Sara Negrello ◽  
Arrigo Pellacani ◽  
Anna Maria Cesinaro ◽  
Stefano Vallone ◽  
...  
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Maxillary Sinus ◽  
Solitary Fibrous Tumor ◽  
Malignant Neoplasm ◽  
Neck Region ◽  
Benign Neoplasm ◽  
Surgical Excision ◽  
Purulent Discharge ◽  
Fibrous Tumor

A solitary fibrous tumor (SFT) is a benign neoplasm, firstly described as a mesenchymal tumor of the pleura. Its incidence range in the head and neck region is about 5–27%, but only rarely does it affect paranasal sinuses. The differential diagnosis is challenging, owing to its erosive growth pattern and immuno-histochemical features. SFTs have an aggressive behavior and an important recurrence potential. Therefore, a radical surgical excision is the gold standard therapeutic procedure. A rare SFT originating from the right maxillary sinus is reported here. The 37-year-old patient presented to the outpatient clinic with a painful expansive lesion in the whole right maxillary region. The overlying skin was inflamed and the patient had no epistaxis episodes. The 1.5 dentary element tested negative for vitality; however, a puncture of the lesion led to a hematic spill and no purulent discharge. An endoscopic-guided biopsy was suggestive either of SFT or hemangioperictoma, excluding a malignant neoplasm. A multi-equipe surgical team was activated. The lesion was embolized in order to achieve a good hemostatic control and, after 48 h, the neoplasm was radically excised with a combined open and endoscopic approach. The patient was disease-free at 12-month radiological and clinical follow-up. Given the rarity of this lesion and the delicacy required in addressing head and neck neoplasms, we believe that the present case report might be of help in further understanding how to approach cranio-facial SFTs.

scholarly journals Papillary cystadenoma of right testis: Case report and literature review

2017 ◽  
Vol 4 (2) ◽  
pp. 8
Author(s):  
Otobo O. Fidelis ◽  
Ikpi Edet ◽  
Enakirerhi Glen ◽  
Isiwele M. Edoise ◽  
Omotosho Ayodele ◽  
...  
Keyword(s):  
Renal Cell Carcinoma ◽  
Case Report ◽  
Malignant Tumors ◽  
Benign Neoplasm ◽  
Adenomatoid Tumor ◽  
Von Hippel Lindau ◽  
Male Undergraduate ◽  
History Of ◽  
Papillary Cystadenoma ◽  
Vhl Disease

Testicular cystadenoma is ranked the second commonest benign neoplasm. Other benign epididymal neoplasms include adenomatoid tumor (most common), leiomyoma, serous (nonpapillary) cystadenoma, cavernous hemangioma, and melanotic neuroectodermal tumor. Adenocarcinoma, mesothelioma, and metastatic renal cell carcinoma are malignant tumors that can affect the epididymis. A 24-year-old male undergraduate with a 3-month history of mildly tender right testicular swelling histologically diagnosed as papillary cystadenoma is presented. This case is presented from our locality as the first of its’ kind; and because it can be a possible manifestation of other diseases like von Hippel- Lindau (VHL) disease.

scholarly journals Vulvar Hemangioma: Case Report

2018 ◽  
Vol 40 (06) ◽  
pp. 369-371
Author(s):  
Janine Silva ◽  
Emily Calife ◽  
João Cabral ◽  
Hildemárzio Andrade ◽  
Ana Gonçalves
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Female Patient ◽  
Surgical Approach ◽  
Benign Neoplasm ◽  
Surgical Excision ◽  
Genital Ulcer ◽  
Emotional Disability ◽  
The Past ◽  
History Of

AbstractHemangioma is a benign neoplasm that may affect the vulva, and it can cause functional or emotional disability. This article reports the case of a 52-year-old female patient with a history of a genital ulcer for the past 3 years and who had undergone various treatments with creams and ointments. The patient was biopsied and diagnosed with vulvar hemangioma and was subsequently submitted to surgical excision of the lesion. We emphasize the importance of following the steps of the differential diagnosis and proceeding with a surgical approach only if necessary.

scholarly journals Báo cáo một trường hợp u cơ trơn nguyên phát ở thận và hồi cứu y văn

2020 ◽  
Author(s):  
Thị Hoài Nam Trịnh
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Renal Tumor ◽  
Benign Neoplasm ◽  
Review Literature ◽  
Solid Mass ◽  
Spindle Cells ◽  
Eosinophilic Cytoplasm

A CASE REPORT OF RENAL LEIOMYOMA AND REVIEW LITERATURE Renal leiomyoma is a benign neoplasm that has been reported frequently in uterus but rarely in kidney. The aim of this study is to show a case report of primary renal leiomyoma and review literature. A 59-year-old female patient presented with an indolent right kidney mass. AbdominalCT Scan showed a well-defined hyperattenuating solid mass, no invade. Microscopically, the lesion showed typical features of leiomyoma, including spindle cells with deeply eosinophilic cytoplasm, arranged in intersecting fascicles. Thetumor cells were diffusely positive with vimentin, SMA and desmin. Keywords: leiomyoma, renal tumor, renal leiomyoma.

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