scholarly journals Inflammatory myofibroblastic tumour of the mandible – A case report

2020 ◽  
Vol 10 (1) ◽  
pp. 21-24
Author(s):  
Mohammad Asifur Rahman
Keyword(s):  
Case Report ◽  
Current Mode ◽  
Surgical Excision ◽  
Clinicopathological Features ◽  
Inflammatory Myofibroblastic Tumour ◽  
Unknown Aetiology ◽  
Maxillofacial Region ◽  
Malignant Lesions ◽  
Extra Pulmonary

Inflammatory myofibroblastic tumour (IMT) is an extremely rare, benign softtissue lesion of unknown aetiology and pathogenesis that mimics malignant lesions clinically and radiologically found in the maxillofacial region. It occurs primarily in the lungs but occurred in other extra-pulmonary sites. Histologically these lesions appear as an inflammatory infiltrate within a variable of myofibrotic background. The current mode of treatment for inflammatory myofibroblastic tumour (IMT) is surgical excision with regular follow up. In this case report a 40 years old female presented with an intraosseous inflammatory myofibroblastic tumour (IMT) in the left side of mandible which was treated by surgical excision of the lesion. This article also describes the clinicopathological features and treatment of a case of inflammatory myofibroblastic tumour (IMT) of the mandible. Update Dent. Coll. j: 2020; 10 (1): 21-24

scholarly journals Giant omental inflammatory myofibroblastic tumour causing intestinal obstruction: a rare care report and review of literature

2020 ◽  
Vol 7 (7) ◽  
pp. 2399
Author(s):  
Utkarsh Kumar ◽  
Gaurav Thami ◽  
Hemlata Kamra ◽  
Nivesh Agarwal
Keyword(s):  
Surgical Excision ◽  
Malignant Potential ◽  
World Health ◽  
Inflammatory Myofibroblastic Tumour ◽  
Unknown Aetiology ◽  
Review Of Literature ◽  
Mesenchymal Tumour ◽  
Complete Surgical Excision ◽  
Health Organization

It is a rare mesenchymal tumour of intermediate biologic potential (according to World Health Organization), with unknown aetiology. It is benign tumour with malignant potential. It frequently recurs and rarely metastasizes. Abdominopelvic inflammatory myofibroblastic tumours have the recurrence rate of 85% so meticulous follow up is necessary. Complete surgical excision is the main stay treatment.

scholarly journals Primary cutaneous CD4+ small/medium T-cell lymphoma: a case report

2021 ◽  
Vol 22 (4) ◽  
pp. 199-203
Author(s):  
Jeenam Kim ◽  
Minkyoung Jeong ◽  
Dongkeun Jun ◽  
Myungchul Lee ◽  
Donghyeok Shin ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Lymphoproliferative Disorder ◽  
Cell Lymphoma ◽  
Surgical Excision ◽  
Lymphoid Cells ◽  
The Face ◽  
Single Mass ◽  
Histopathologic Findings

Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder is a rare disease characterized by a single mass on the face or upper part of the trunk. It usually presents an asymptomatic and favorable progression, and its histopathologic findings include small and medium-sized lymphoid cells. The authors report a case of primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder on the forehead. A 51-year-old man presented with a protruding mass on his forehead that the patient had noted 1 month previously. Surgical excision and a permanent biopsy were performed under local anesthesia. Based on the biopsy results, the mass was diagnosed as a primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder. There was no evidence of recurrence at a 15-month follow-up visit.

scholarly journals Huge true aneurysm of the facial artery treated with internal trapping and surgical excision: a case report

2020 ◽  
Vol 2020 (9) ◽  
Author(s):  
Kiyoko Nakagawa ◽  
Takuji Yasuda ◽  
Natsuko Kobayashi ◽  
Kazuhiko Urabe
Keyword(s):  
Case Report ◽  
Case Reports ◽  
Surgical Excision ◽  
Facial Artery ◽  
True Aneurysm ◽  
The Right

Abstract A report of true aneurysms is extremely rare. There are only five previous case reports of true aneurysm of the facial artery. In the previously reported cases, there was no case that underwent trapping and surgical excision. In this case report, we describe the procedure of internal trapping before the surgical excision of a huge true aneurysm of the right facial artery for a 79-year-old woman. There was no recurrence of the aneurysm during a 6-month follow-up period.

Role of contrast-enhanced spectral mammography in the post biopsy management of B3 lesions: Preliminary results

2018 ◽  
Vol 105 (5) ◽  
pp. 378-387 ◽  
Author(s):  
Giulia Bicchierai ◽  
Jacopo Nori ◽  
Diego De Benedetto ◽  
Cecilia Boeri ◽  
Ermanno Vanzi ◽  
...  
Keyword(s):  
Breast Imaging ◽  
Surgical Excision ◽  
Surgical Biopsy ◽  
Predictive Values ◽  
Contrast Enhanced ◽  
B3 Lesions ◽  
Malignant Lesions ◽  
Sensitivity Specificity

PurposeTo evaluate the role of contrast-enhanced spectral mammography (CESM) in the post biopsy management of breast lesions classified as lesions of uncertain malignant potential (B3) by core needle biopsy and vacuum-assisted biopsy (VAB).MethodsThe local ethics committee approved this retrospective study and for this type of study formal consent is not required. A total of 42 B3 lesions in 40 women aged 41–77 years were included in our study. All patients underwent CESM 2–3 weeks after the biopsy procedure and surgical excision was subsequently performed within 60 days of the CESM procedure. Three radiologists reviewed the images independently. The results were then compared with histologic findings.ResultsThe sensitivity, specificity, and positive and negative predictive values for confirmed demonstration of malignancy at CESM were 33.3%, 87.2%, 16.7%, and 94.4% for reader 1; 66.7%, 76.9%, 18.2%, and 96.7% for reader 2; 66.7%, 74.4%, 16.7%, and 96.7% for reader 3. Overall agreement on detection of malignant lesions using CESM among readers ranged from moderate to substantial (κ = .451–.696), for categorization of BPE from moderate to substantial (κ = .562–.711), and for evaluation of lesion intensity enhancement from fair to moderate (κ = .346–.459).ConclusionIn cases of Breast Imaging Reporting and Data System (BI-RADS) 1, BI-RADS 2, or BI-RADS 3 results at CESM, follow-up or VAB rather than surgical biopsy might be performed.

Well-differentiated liposarcoma arising in the parapharyngeal space: a case report and review of the literature

2015 ◽  
Vol 129 (S2) ◽  
pp. S86-S90 ◽  
Author(s):  
N Kikuchi ◽  
T Nakashima ◽  
J Fukushima ◽  
K Nariyama ◽  
S Komune
Keyword(s):  
Case Report ◽  
Parapharyngeal Space ◽  
Case Reports ◽  
Surgical Margin ◽  
Neck Region ◽  
Surgical Excision ◽  
Curative Therapy ◽  
Long Term Follow Up ◽  
Well Differentiated

AbstractBackground:Liposarcomas rarely occur in the parapharyngeal space and only a few case reports exist. For curative therapy of liposarcoma, surgical excision remains the dominant modality. Although a wide surgical margin is important to prevent local recurrence, wide excision is often difficult in the head and neck region.Case report:We report a case of a 19-year-old female with a well-differentiated liposarcoma arising in the parapharyngeal space. We removed the tumour surgically utilising a cervical–parotid approach. The histological diagnosis was well-differentiated sclerosing liposarcoma. There is no recurrence after five years and nine months of follow up.Conclusion:The patient's age and the tumour site made it difficult for us to make a quantitative diagnosis before the operation. Well-differentiated liposarcoma rarely develop distant metastasis, but often recur locally. The benefit of adjuvant radiotherapy for well-differentiated liposarcoma is still not clear and careful and long-term follow up is necessary.

Treatment of piriform fossa sinuses with monopolar diathermy

2007 ◽  
Vol 122 (8) ◽  
pp. 840-844 ◽  
Author(s):  
J Ahmed ◽  
S De ◽  
I D B Hore ◽  
C M Bailey ◽  
B E J Hartley
Keyword(s):  
Case Report ◽  
Treatment Modality ◽  
Surgical Excision ◽  
Internal Opening ◽  
Effective Management ◽  
Management Option ◽  
Retrospective Case ◽  
Traditional Management ◽  
Sinus Opening

AbstractIntroduction:Embryological remnants of third or fourth branchial pouches are a rare but important cause of recurrent neck abscesses in children. They are characterised by an internal opening in the piriform fossa. Traditional management involves surgical excision of the entire tract. We present our experience with the use of monopolar diathermy applied to the internal sinus opening as a treatment modality for this condition.Materials and methods:A retrospective, case report review was performed.Results:Four cases of piriform fossa sinus were treated with monopolar diathermy to the sinus opening via an endoscopic approach. The first three cases were treated in this way for recurrence, following external tract excision, while the fourth case had simultaneous excision of the tract and diathermy to the piriform fossa opening. There were no serious complications and no recurrence within a follow-up period ranging from nine to 27 months.Discussion:Obliteration of the internal opening of these sinuses by endoscopic diathermy is a safe and effective management option for this condition, either as an alternative to or as an adjunct to external surgical excision of the tract.

Surgical excision of large ameloblastic fibro-odontoma followed by alloplastic bone graft—2 year follow-up: A case report

2015 ◽  
Vol 27 (1) ◽  
pp. 41-44 ◽  
Author(s):  
Divesh Sardana ◽  
Vidya Rattan ◽  
Krishan Gauba ◽  
Ashima Goyal ◽  
Satnam Singh ◽  
...  
Keyword(s):  
Case Report ◽  
Bone Graft ◽  
Surgical Excision

scholarly journals Mucocele of the glands of blandin nuhn: a case report

2013 ◽  
pp. 46-47 ◽  
Author(s):  
Nathalia García-León ◽  
Gilberto E Marrugo
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Clinical Presentation ◽  
Surgical Excision ◽  
Diagnosis And Treatment ◽  
Vascular Lesions ◽  
Benign Lesions ◽  
Recurrent Lesion ◽  
Timely Diagnosis

Mucoceles arising from the Blandin Nuhn glands are uncommon benign lesions of the oral cavity, which by their clinical presentation may be confused with more serious diseases such as vascular lesions, pyogenic granulomas, polyps, or squamous papillomas; thereby, it is convenient to be aware of the characteristics of this entity to guide the accurate and timely diagnosis and treatment. Herein, we present a case of a 10-year-old patient with a recurrent lesion of this type, which required surgical excision and marsupialization of the same, with no evidence of recurrence during follow-up.

Odontogenic Myxoma – A Case Report and Clinico-Radiographic Study of Seven Tumors

2006 ◽  
Vol 7 (1) ◽  
pp. 117-124 ◽  
Author(s):  
Mariela Siqueira Gião Dezotti ◽  
Luciana Reis Azevedo ◽  
Flávia Noemi Gasparini Kiatake Fontão ◽  
Ana Lůcia Ålvares Capelozza ◽  
Eduardo Sant'ana
Keyword(s):  
Case Report ◽  
Root Resorption ◽  
Surgical Excision ◽  
Radiographic Study ◽  
Odontogenic Myxoma ◽  
Appropriate Treatment ◽  
Dental Records ◽  
School Of Dentistry ◽  
Radiographic Result

Abstract The primary aim of this paper is to present clinical and radiographic aspects of odontogenic myxomas diagnosed at the Stomatology Clinic of Bauru School of Dentistry, University of São Paulo, Brazil and to compare them with data reported in a series published in the literature. A second objective is to report a clinical case of odontogenic myxoma in a 9-year-old patient in whom the lesion involved the anterior region of the maxilla. Dental records between 1975 and 2000 were reviewed and seven cases diagnosed as odontogenic myxoma were found in individuals aged from nine to 60 years. Of these, four occurred in women and three in men. The mandible was affected in five cases and the maxilla in two. All patients presented with asymptomatic swelling in the affected area. A mixed radiographic result was observed in five patients, while in two patients the lesion was completely radiolucent. The borders of the lesion were well-defined in six patients. In four cases there was dental displacement, although root resorption was not observed in any of these. The treatment of choice was surgical excision. Four cases did not recur during the period of follow-up, which varied from nine months to 19 years. It was concluded the clinico-radiographic study of odontogenic myxomas should be continually refined with the aim of offering the patient an appropriate treatment, since the lesion presents a high potential for recurrence. Citation Dezotti MSG, Azevedo LR, Fontão FNGK, Capelozza ALA, Sant'ana E. Odontogenic Myxoma – A Case Report and Clinico-Radiographic Study of Seven Tumors. J Contemp Dent Pract 2006 February;(7) 1:117-124.

Treatment of pregnancy-associated oral pyogenic granuloma with life-threatening haemorrhage by transarterial embolisation

2015 ◽  
Vol 129 (6) ◽  
pp. 607-610 ◽  
Author(s):  
K-Y Tsai ◽  
W-H Wang ◽  
G-H Chang ◽  
Y H Tsai
Keyword(s):  
Case Report ◽  
Pregnant Woman ◽  
Surgical Excision ◽  
Pyogenic Granuloma ◽  
Severe Bleeding ◽  
Transarterial Embolisation ◽  
Wound Pain ◽  
Life Threatening ◽  
One Year

AbstractBackground:Pregnancy-associated pyogenic granuloma (pregnancy tumour) is not uncommon. However, control of severe bleeding associated with the lesion by transarterial embolisation has never been reported.Case report:We report the case of a 33-year-old pregnant woman (34 weeks gestation) who presented with a pregnancy-associated pyogenic granuloma of the mandibular gingiva with a life-threatening haemorrhage. The bleeding stopped soon after transarterial micro-embolisation and regressed after one month; thus, no further surgical excision was needed. The patient was free of post-operative wound pain and infection, and there was no recurrence after one year of follow up.Conclusion:In general, surgical excision is the first treatment choice for pregnancy tumours. However, it is limited by the risk of marked deformity or incomplete excision when large lesions or difficult surgical areas are encountered. For large tumours, transarterial embolisation may be a safer alternative.

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