A fetus with a huge neck mass and a large abdominal circumference - a rare case of sialoblastoma and hepatoblastoma

2012 ◽  
pp. 1-3
Author(s):  
Yvonne Kwun-Yue Cheng ◽  
Winnie Chiu-Wing Chu ◽  
Lai Wa Law ◽  
Yuen Ha Ting ◽  
Tak Yeung Leung
Keyword(s):  
Rare Case ◽  
Neck Mass ◽  
Abdominal Circumference

scholarly journals A rare case of infiltrative hepatocellular carcinoma presented with neck mass

2020 ◽  
Author(s):  
Yu‐Kwang Lee ◽  
Chung‐Chieh Wang ◽  
Yu‐Tse Chiu ◽  
Tai‐Chung Tseng
Keyword(s):  
Hepatocellular Carcinoma ◽  
Rare Case ◽  
Neck Mass

scholarly journals Castleman's Disease: An Orphan Lymphoproliferative Disorder

2015 ◽  
Vol 6 (1) ◽  
pp. 20-22
Author(s):  
Pratik Dipak Shah ◽  
Srijon Mukherji ◽  
Yogendra Chauhan
Keyword(s):  
Lymphoproliferative Disorder ◽  
Rare Case ◽  
Castleman’S Disease ◽  
Neck Mass ◽  
Benign Disease ◽  
Castleman's Disease ◽  
Unusual Site ◽  
Reactive Lymph Node ◽  
Head Neck ◽  
Lymph Node Hyperplasia

ABSTRACT Castleman's disease (CD) is a rare, benign disease of unknown cause that induces reactive lymph node hyperplasia. The disease was first defined by Dr Benjamin Castleman. It is an unusual cause of a neck mass. The goal of this paper is to report a rare case of Castleman's disease at unusual site (level IB) and discuss its management. How to cite this article Shah PD, Chauhan Y, Mukherji s. Castleman's Disease: An Orphan Lymphoproliferative Disorder. Int J Head Neck Surg 2015;6(1):20-22.

scholarly journals A Case of Masson’s Tumor in Lateral Neck

2020 ◽  
Vol 63 (11) ◽  
pp. 541-544
Author(s):  
Hoyoung Lee ◽  
Soo Jeong Choi ◽  
In Hak Choi ◽  
Kwang Yoon Jung
Keyword(s):  
Endothelial Cells ◽  
Differential Diagnosis ◽  
Rare Case ◽  
Vascular Tumor ◽  
Neck Mass ◽  
Lateral Neck ◽  
Intravascular Papillary Endothelial Hyperplasia ◽  
Masson’S Tumor ◽  
Papillary Endothelial Hyperplasia ◽  
The Right

Masson’s tumor, also known as intravascular papillary endothelial hyperplasia (IPEH), is a rare, benign vascular tumor characterized by the proliferation of endothelial cells with papillary formations. Differential diagnosis between IPEH and angiosarcoma is important because both have microscopic similarity. Herein, we report a rare case of IPEH on the right lateral neck of a 50-year-old female presenting with a neck mass, which was completely removed without complication.

Intramuscular Hemangioma of the sternocleidomastoid muscle: A Rare Unusual Neck Mass

2020 ◽  
Vol 13 (1) ◽  
pp. 78-82
Author(s):  
Brihaspati Sigdel ◽  
Rajesh Maharjhan ◽  
Tulika Dubey ◽  
Bhima Neupane
Keyword(s):  
Head And Neck ◽  
Rare Case ◽  
Neck Region ◽  
Neck Mass ◽  
Sternocleidomastoid Muscle ◽  
Benign Tumors ◽  
Head And Neck Region ◽  
Intramuscular Hemangioma ◽  
Slow Growing ◽  
Extensive Involvement

Hemangiomas of the head and neck region comprise about 60 to 70% of all benign tumors. Intramuscular hemangioma is a rare, slow-growing, angiomatous tumor. We report a rare case of an Intramuscular Hemangioma of Right sternocleidomastoid muscle in a six years old girl presenting for four years and with extensive involvement necessitating excision. Microscopic excision reduces the risk of recurrence.

Cryptococcosis Presenting as a Neck Mass

1995 ◽  
Vol 104 (9) ◽  
pp. 711-714 ◽  
Author(s):  
David M. Schmidt ◽  
Kevin F. Kevorkian ◽  
Joel A. Sercarz ◽  
Rinaldo F. Canalis
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Healthy Individual ◽  
Complete Resolution ◽  
Rare Case ◽  
Cervical Vertebrae ◽  
Neck Mass ◽  
Upper Extremities ◽  
Cryptococcal Infection ◽  
Focal Neurologic Deficit

A rare case of cryptococcal infection presenting as a neck mass in an otherwise healthy individual is reported. The mass resulted in lytic destruction of portions of the cervical vertebrae and produced a focal neurologic deficit in one of the upper extremities. Although other lesions in the skull, femur, and humerus were identified, no involvement of the lungs or central nervous system could be detected. The patient was initially treated with amphotericin B and flucytosine, but eventually also required fluconazole and surgical debridement for complete resolution of the infection. The diagnosis, treatment, and manifestations of cryptococcosis in the head and neck are discussed.

scholarly journals A rare case of extracranial meningioma in parapharyngeal space presented as a neck mass

2015 ◽  
Vol 11 ◽  
pp. 40-43 ◽  
Author(s):  
Nader Albsoul ◽  
Badi Rawashdeh ◽  
Ahmad Albsoul ◽  
Mohammad Abdullah ◽  
Simin Golestani ◽  
...  
Keyword(s):  
Rare Case ◽  
Parapharyngeal Space ◽  
Neck Mass ◽  
Extracranial Meningioma

scholarly journals A Rare Case of Vagus Nerve Schwannoma Presenting as a Neck Mass

2017 ◽  
Vol 18 ◽  
pp. 908-911 ◽  
Author(s):  
Adesh A. Ramdass ◽  
Mike Yao ◽  
Suneetha Natarajan ◽  
Parampreet K. Bakshi
Keyword(s):  
Vagus Nerve ◽  
Rare Case ◽  
Neck Mass

scholarly journals A RARE CASE OF A GIANT HEMANGIOENDOTHELIOMA OF NECK

2015 ◽  
Vol 23 (3) ◽  
pp. 120-122
Author(s):  
Swagatam Banerjee ◽  
Sharmistha Chakravarty ◽  
Saurav Sarkar ◽  
Sankar Prasad Bera
Keyword(s):  
Rare Case ◽  
Clinical Presentation ◽  
Parapharyngeal Space ◽  
Histopathological Examination ◽  
Neck Mass ◽  
Tumour Mass ◽  
Large Tumour ◽  
Soft Tissue Neoplasm ◽  
Borderline Tumour ◽  
Posterior Triangle

Introduction Hemangioendothelioma is a rare variety of vascular soft tissue neoplasm, classified as a borderline tumour with diverse modality of clinical presentation. It is seen mostly at sites like the liver, lungs and bones while very few head and neck cases have been reported.                          Case Report A rare case of an unusually large tumour mass presenting as an anterolateral neck mass with extensions to right parapharyngeal space, posterior triangle and prevertebral space is presented here. The entire tumour was removed en-masse surgically. Histopathological examination confirmed the mass to be an epitheloid hemangioendothelioma, the enormous size of which in the neck makes it unique and unusual.

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