scholarly journals Retroperitoneal Plasmacytoma: A Case Report

2012 ◽  
Vol 30 (3) ◽  
pp. 167-169
Author(s):  
SM Amjad Hossain ◽  
Mohammad Rafiz Imtiaz ◽  
Gopal Verma
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Neck Region ◽  
Extramedullary Plasmacytoma ◽  
Elderly Male ◽  
College Hospital ◽  
Head And Neck Region ◽  
First Report ◽  
Rare Neoplasm ◽  
Medical College

Solitary Extramedullary Primary Plasmacytoma (SEMPP) is a rare neoplasm. When diagnosed, head and neck region is its most likely location. Rarely, it may occur in the retroperitoneum. We report a case of an elderly male who  was admitted in the department of surgery, Dhaka Medical College Hospital (DMCH) with a Solitary Extramedullary  Retroperitoneal Primary Plasmacytoma (SEMRPP). Subtotal excision of the mass was done. The patient was referred to the department of Oncology DMC for radiotherapy. The first report of an extramedullary plasmacytoma was in 1905 in Taiwan. To the best of our knowledge, there was no report of a Solitary Extramedullary Retroperitoneal Primary Plasmacytoma (SEMRPP) from Bangladesh.DOI: http://dx.doi.org/10.3329/jbcps.v30i3.12467 J Bangladesh Coll Phys Surg 2012; 30: 167-169

scholarly journals Multiple Extramedullary Plasmacytoma Arising in the Head and Neck Region; A Case Report.

1996 ◽  
Vol 89 (11) ◽  
pp. 1377-1381 ◽  
Author(s):  
Sanson HAN ◽  
Hiroyuki KITAMURA ◽  
Shin-ichi TAKAGITA ◽  
Ryo ASATO ◽  
Yuka IWAHASHI ◽  
...  
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Neck Region ◽  
Extramedullary Plasmacytoma ◽  
Head And Neck Region

Combined modality therapy for naso-oropharyngeal solitary extramedullary plasmacytoma: case report

2017 ◽  
Vol 3 (4) ◽  
pp. 1105
Author(s):  
Andrea Masarykova ◽  
Marin Dzongov ◽  
Alexandra Hanicova ◽  
Ingrid Zavacka ◽  
Danijela Scepanovic
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Plasma Cell ◽  
Fdg Pet ◽  
Neck Region ◽  
Extramedullary Plasmacytoma ◽  
Head And Neck Region ◽  
Pet Ct ◽  
Fdg Pet Ct ◽  
Solitary Extramedullary Plasmacytoma

<p>Most patients with plasma cell neoplasia have generalized disease at diagnosis. However, some patients have a solitary extramedullary plasmacytomas (SEPs). SEPs are rare, typically solitary tumors comprising approximately 3–5% all plasma cell neoplasms. Almost 90% arise in the head and neck region, especially in the nasal cavity, sinuses, oropharynx, salivary glands and larynx. Solitary extramedullary plasmacytoma (SEP) has a predilection for the male gender and occurs most frequently in patients 50 years and older. SEP often runs an indolent clinical course with a tendency for local recurrence, and progresses to plasma cell myeloma in about 15% of patients. In this paper, we have reported the case of SEP of the naso-oropharynx in 55 years old woman who was presented with a sense of the nasal obstruction. The resection was performed and a mature plasmacytoma was demonstrated histologically. However, ENT examination and positron emission tomography/computed tomography examination with 18-fluorodeoxyglucose (18-FDG PET/CT) have shown that the patient had residual naso-oropharyngeal disease after surgery. A negative bone marrow biopsy and 18-FDG PET/CT have confirmed that it was a solitary extramedullary plasmacytoma of the head and neck region. Following the surgery, intensity modulated radiotherapy (IMRT) was administered. No relapse or progression to the multiple myeloma was recorded during the 3.5 years of follow-up. This case report, which describes a rare tumor of the naso-oropharynx, is expected to improve the recognition and referral of this condition in medical practice. </p>

scholarly journals Concomitant cemento-osseous dysplasia and aneurysmal bone cyst of the mandible: a rare case report with literature review

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Han-Gyeol Yeom ◽  
Jung-Hoon Yoon
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Aneurysmal Bone Cyst ◽  
Cystic Lesion ◽  
Bone Cyst ◽  
Neck Region ◽  
Diagnostic Process ◽  
Simultaneous Occurrence ◽  
Head And Neck Region ◽  
Osseous Dysplasia

Abstract Background Concomitant cemento-osseous dysplasia (COD) and aneurysmal bone cyst (ABC) are rare in the head and neck region. In our search of the English language literature, we found only one case report describing the simultaneous occurrence of COD and ABC in the head and neck region. Here, we report a case of COD associated with ABC. Further, we performed a systematic search of the literature to identify studies on patients with COD associated with nonepithelial lined cysts of the jaws. Case presentation The patient was a 32-year-old woman who was referred from a private dental clinic because of a cystic lesion below the mandibular right first molar. She had no pain or significant systemic disease. After performing panoramic radiography and cone-beam computed tomography, the imaging diagnosis was COD with a cystic lesion, such as ABC or solitary bone cyst. Excisional biopsy was performed, which revealed concomitant COD and ABC. Conclusion This case of ABC associated with COD provides insight for the diagnostic process of radiographically mixed lesions with cystic changes.

scholarly journals Asymptomatic Presentation of Aggressive Ossifying Fibroma:A Case Report

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Roopashri Rajesh Kashyap ◽  
Gopakumar R. Nair ◽  
Subhas Babu Gogineni
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Head And Neck ◽  
Clinical Symptoms ◽  
Neck Region ◽  
Ethmoid Sinus ◽  
Ossifying Fibroma ◽  
Head And Neck Region ◽  
Aggressive Form ◽  
Aggressive Tumors

Ossifying fibromas form a part of the spectrum of fibro-osseous lesions of the jaws. They are rare, benign, nonaggressive tumors that are commonly seen in head and neck region. This paper presents the case of a 40-year-old female patient presented with minimal clinical symptoms, diagnosed to be suffering from aggressive form of ossifying fibroma of maxilla involving the maxillary sinus and ethmoid sinus. This paper emphasizes the importance of computed tomography in diagnosing such unapparent aggressive tumors.

scholarly journals A case report of giant anterior neck lipoma

2020 ◽  
Vol 6 (6) ◽  
pp. 1213
Author(s):  
Shalini Jain ◽  
Sahil Maingi ◽  
Ancy S. Sofia ◽  
A. K. Rai
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Neck Region ◽  
Surgical Excision ◽  
The Body ◽  
Anterior Neck ◽  
Head And Neck Region ◽  
Posterior Triangle ◽  
Common Location ◽  
Different Parts

<p class="abstract">Lipoma is a benign mesenchymal tumor with a thirteen percent incidence in head and neck region. Posterior triangle is the most common location while anterior neck lipoma is a rare one. Giant lipomas &gt;10 cm have been reported in different parts of the body but rarely in the anterior neck. Surgical excision remains the treatment of choice. We here report a case of giant anterior neck lipoma in a 50 year old male managed surgically.</p>

scholarly journals Omental lymphangioma: a rare case report

2020 ◽  
Vol 10 (3) ◽  
pp. 106-108
Author(s):  
Geha Raj Dahal
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Rare Case ◽  
Neck Region ◽  
Mass Effect ◽  
Complete Excision ◽  
Benign Condition ◽  
Head And Neck Region ◽  
Rare Case Report

Lymphangioma is a common pediatric problem. Most of the lymphangiomas occur in head and neck region. Lymphangioma arising from omentum is extremely rare. It is a benign condition butis locally invasive. Symptoms usually arise from its mass effect or complications. Complete excision including removal of all loculi is necessary for cure. We report such a case of omental lymphangiomain a six-year boy.

Leiomyosarcoma of the auricle: case report and literature review

1998 ◽  
Vol 112 (2) ◽  
pp. 166-168 ◽  
Author(s):  
R. Murat Karasen ◽  
Yavuz Sutbeyaz ◽  
Cemal Gundogdu ◽  
Bulent Aktan
Keyword(s):  
Smooth Muscle ◽  
Case Report ◽  
Literature Review ◽  
Head And Neck ◽  
External Auditory Canal ◽  
Neck Region ◽  
Malignant Tumour ◽  
Head And Neck Region ◽  
Muscle Origin

AbstractLeiomyosarcoma is a malignant tumour of smooth muscle origin. These tumours are rarely encountered in the head and neck region. A case of leiomyosarcoma of the auricle is presented. There are two cases of external auditory canal leiomyosarcoma in the literature. To our knowledge the present case is the first example of leiomyosarcoma of the auricle.

scholarly journals Rhabdomyosarcoma of the Oral Cavity: A Case Report

2011 ◽  
Vol 05 (03) ◽  
pp. 340-343 ◽  
Author(s):  
Ozkan Miloglu ◽  
Sare Sipal Altas ◽  
Mustafa Cemil Buyukkurt ◽  
Burak Erdemci ◽  
Oguzhan Altun
Keyword(s):  
Skeletal Muscle ◽  
Case Report ◽  
Soft Tissue ◽  
Oral Cavity ◽  
Head And Neck ◽  
Soft Tissues ◽  
Neck Region ◽  
Childhood And Adolescence ◽  
Head And Neck Region ◽  
The Common

ABSTRACTRhabdomyosarcoma (RMS), a tumor of skeletal muscle origin, is the most common soft tissue sarcoma encountered in childhood and adolescence. The common sites of occurrence are the head and neck region, genitourinary tract, retroperitonium, and, to a lesser extent, the extremities. In the head and neck region, the most commonly affected sites are the orbit, paranasal sinuses, soft tissues of the cheek, and the neck. RMS is relatively uncommon in the oral cavity, and the involvement of the jaws is extremely rare. Here, we report a case of oral RMS in a 13-year-old child and describe the clinical, radiological, histopathological, and immunohistochemical findings. (Eur J Dent 2011;5:340-343)

scholarly journals Giant locally advanced and metastatic squamous cell skin carcinoma of head and neck region: case report

2020 ◽  
Vol 25 (1) ◽  
pp. 20-22
Author(s):  
Jan Stuk ◽  
Jaroslav Vanasek ◽  
Karel Odrazka ◽  
Martin Dolezel ◽  
Iveta Kolarova ◽  
...  
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Squamous Cell ◽  
Locally Advanced ◽  
Neck Region ◽  
Skin Carcinoma ◽  
Head And Neck Region ◽  
Squamous Cell Skin Carcinoma

scholarly journals Extraoral Osseous Choristoma in the Head and Neck Region: Case Report and Literature Review

2019 ◽  
Vol 2019 ◽  
pp. 1-3
Author(s):  
Philipp Arens ◽  
Andrea Ullrich ◽  
Heidi Olze ◽  
Florian Cornelius Uecker
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Literature Review ◽  
Head And Neck ◽  
Benign Tumor ◽  
Neck Region ◽  
Cervical Tumor ◽  
Submandibular Region ◽  
Head And Neck Region ◽  
Important Differential Diagnosis

An osseous choristoma is a benign tumor consisting of regular bone tissue in an irregular localization. Choristomas in the head and neck region are rare. Most frequently, they are found in the region of the tongue or oral mucosa. There are also very few reports on osseous choristomas in the submandibular region. We present the case of a woman with a large, caudal osseous choristoma within the lateral cervical triangle. Literature review is given about all of the reported cases in the region of the neck. The pathogenesis is yet unexplained. Our case supports the theory that the development of an osseous choristoma is a reaction to a former trauma. Cervical osseous choristomas are seldom, but they represent an important differential diagnosis when dealing with a cervical tumor.

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