Infratemporal hydatid cyst – unusual location of echinococcosis

1994 ◽  
Vol 108 (7) ◽  
pp. 601-603 ◽  
Author(s):  
Levent Sennaroḡlu ◽  
Metin ÖNercĩ ◽  
Ergĩn Turan ◽  
Arzu Sungur

AbstractHydatid disease is an important medical problem in countries of the temperate zones. Only occasional cases are reported in the head and neck region. An unusual location for hydatid disease in the infratemporal fossa is presented. Characteristics of this rare disease together with treatment modalities are discussed.

1996 ◽  
Vol 110 (10) ◽  
pp. 978-980 ◽  
Author(s):  
K. Gangopadhyay ◽  
M. O. Abuzeid ◽  
H. Kfoury

AbstractHydatid disease is caused by the parasitic tapeworm Echinococcus. This parasite in larval stage can thrive in many parts of the body, most commonly in the liver and the lung. Hydatid disease in the head and neck region is rare. An unusual location for hydatid disease in the pterygopalatine fossa-infratemporal fossa is presented. The patient did not have evidence of any other cyst on a ten-year follow-up.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Hetal Marfatia ◽  
Nilam U. Sathe ◽  
Subodh Hosagadde ◽  
Keya Shah

Isolated involvement of the orbit by hydatidosis is extremely rare. It is a parasitic infestation due to a tapeworm called <em>Echinococcus Granulosus</em>. It is an uncommon disease in head and neck region as it commonly manifests in the lungs and liver. When seen in head and neck, it has been found in the orbit, paranasal sinuses and salivary glands. Orbital hydatidosis per se forms only 1% of all types of hydatid disease. It is endemic in Africa, Middle East and Southeast Asian countries including India. In orbital hydatid disease, patients usually present with unilateral proptosis and diminution of vision. Proptosis is classically painless. Total surgical removal remains the mainstay of treatment. A 30-year-old female belonging to lower socio-economic status, presented with left eye proptosis since 2 years. There was a gradual increase in proptosis associated with diminution of vision over the last 4 months. This finally led to complete loss of vision in a period of two months. Computed tomography scan showed two soft homogenous non-enhancing cystic structures present in the orbit abutting the optic nerve without any intracranial extension; most likely differentials are a developmental cyst, hydatid cyst, epidermoid cyst, rhabdomyosarcoma or a nerve sheath tumor. Magnetic resonance imaging showed two T1 hypointense non-enhancing, T2 hyperintense soft cystic capsulated space-occupying lesions present in the extraconal compartment of orbit abutting the optic nerve, likely to be lymphangioma or a hydatid cyst. Surgery was planned and endoscopic orbital decompression was done. Sago grain-like granules were seen pouring out of the cysts. Cyst walls were completely removed in piecemeal and the specimen was sent for histopathology. Immediate intra-operative reduction of proptosis was seen. The final histopathological report was suggestive of hydatid cyst.


2021 ◽  
Vol 12 (3) ◽  
pp. e0022
Author(s):  
Muddasir Bhati ◽  
◽  
Gurukeerthi Balakrishna ◽  
Kamaldeep Joshi ◽  
Kajari Bhattacharya ◽  
...  

Objective: The objective of this study was to retrospectively review clinical data, management protocols, and clinical outcomes of patients with fibromatoses of head and neck region treated at our tertiary care center. Methods: We retrospectively reviewed the medical records of 11 patients with confirmed histopathological diagnosis of fibromatosis registered in the Department of Head and Neck Surgery at Tata Memorial Centre, India, between 2009 and 2019. Various clinical and pathological features and treatment modalities were evaluated. Results: Age at diagnosis ranged between 18 and 74 years, with a median age of 36 years. The female-to-male ratio was 5:6. Supraclavicular fossa (n=4) was the most common subsite of origin in the neck (n=8). The lateral (n=2) and posterior cervical regions (n=2) were other common neck subsites. Less commonly involved sites were the mandible (n=1), maxilla (n=1), and thyroid (n=1). A total of eight patients underwent surgery at other centers before being referred to us for further management. Out of a total 11 patients, nine patients had unresectable disease at presentation. Six of the patients with unresectable disease received a combination of weekly doses of vinblastine 6 mg/m2 and methotrexate 30 mg/m2 for a median duration of 6 months (range 6–18 months) followed by hormonal therapy with tamoxifen. Three patients received metronomic chemotherapy followed by hormonal therapy. One treatment-naive patient with fibromatosis of posterior cervical (suboccipital) region underwent R2 resection (excision of bulk of the tumor with preservation of critical structures) at our center along with adjuvant radiotherapy. One pregnant patient reported to us after undergoing surgery outside and defaulting radiotherapy. During median follow-up of 29 months (range 1–77 months), six patients had stable disease, and four patients had disease reduction. Disease progression was seen in one patient. The two-year progression-free survival (PFS) was 90% (95% CI 70%–100%). Conclusion: Gross residual resection (R2) was the mainstay of surgical treatment in our series, as obtaining clear surgical margins is seldom possible in these locally aggressive tumors. Radiotherapy, chemotherapy, and hormonal therapy are the other preferred and more conservative treatment modalities. The goal of surgery should be preserving function with minimal or no morbidity. As fibromatoses in the head and neck region are extremely rare, their treatment awaits the development of standard treatment protocols.


1998 ◽  
Vol 112 (12) ◽  
pp. 1199-1201 ◽  
Author(s):  
Neena Chaudhary ◽  
Anurag Jain ◽  
Sanjay Gudwani ◽  
Rajeev Kapoor ◽  
Gul Motwani

AbstractIntramuscular haemangiomas are rare benign haemangiomas occurring within the skeletal muscle. These are uncommon tumours in the head and neck region and occur most frequently on the trunk and extremities. Fewer than 80 cases of intra-muscular haemangioma in the head and neck region have been reported in the literature.A case of intramuscular haemangioma of the sternocleidomastoid muscle is presented. The review of occurrence and natural history of such tumours is described and clinical and radiological presentation, histological classifications and treatment modalities are discussed.


2004 ◽  
Vol 118 (1) ◽  
pp. 62-64 ◽  
Author(s):  
Yoon Soo Yang ◽  
Ki Hwan Hong

Primitive neuroectodermal tumour/extraskeletal Ewing’s sarcoma (PNET/EES) is a rare disease of the head and neck region. We report a case of a 74-year-old man with a laryngeal Ewing’s sarcoma. This is the first reported case of extraskeletal Ewing’s sarcoma of the larynx in an elderly male patient. The patient was successfully treated with surgical resection and post-operative radiotherapy.


2015 ◽  
Vol 129 (S2) ◽  
pp. S83-S85 ◽  
Author(s):  
R Yasumatsu ◽  
T Nakashima ◽  
M Yamauchi ◽  
S Toh ◽  
S Komune

AbstractPurpose:The management of extrapulmonary small cell carcinoma has not been standardised to date. This study reviewed the clinical course, management and survival outcomes of patients with extrapulmonary small cell carcinoma in the head and neck region.Methods:Nine patients with extrapulmonary small cell carcinoma in the head and neck were included in this study.Results:Five patients received radical surgery followed by adjuvant chemotherapy or radiotherapy or both. Two other patients were treated with chemotherapy consisting of CPT11 plus cisplatin or CPT11 plus cisplatin plus VP-16 three times. Two other patients received chemoradiotherapy consisting of S-1 or CPT11 plus cisplatin. The median overall survival was 14.5 months, with a three-year survival rate of 23.7 per cent.Conclusions:The prognosis of extrapulmonary small cell carcinoma is generally poor. Further prospective multicentre studies are required for better understanding of disease entities and response to treatment modalities.


1998 ◽  
Vol 3 (3) ◽  
pp. 13-14
Author(s):  
M. M. Sathekge ◽  
M. N. Muthuphei ◽  
I. Mandiwana

Hydatid disease is caused by the parasitic tapeworm, Echinococcus granulosus. This parasite in the larval stage can thrive in many parts of the body, most commonly in the liver and the lungs. Hydatid disease in the head and neck region is rare. An unusual location for hydatid disease in the thyroid gland is presented. The patient did not have other cysts postoperatively. The authors state the diagnostic difficulties caused by the omission of sonography during the diagnostic approach.


2011 ◽  
Vol 4 (2) ◽  
pp. 107-109 ◽  
Author(s):  
Somanath B Megalamani ◽  
Deepak Balasubramanium ◽  
Surianarayana Gopalakrishnan ◽  
Sunil Kumar Saxena

ABSTRACT Hydatid disease is a parasitic infestation by a tapeworm of the genus Echinococcus. The disease is endemic in the Middle East, the South Asia and South America. The larvae usually cause cystic lesions in the lung and liver. Hydatid cysts are known to affect the head and neck region. The presence of this cyst in the maxillary sinus is extremely rare and should be suspected in cases presenting from endemic countries.


Author(s):  
Anagha R. Joshi ◽  
Ashwini Sankhe ◽  
Soniya H. Patankar ◽  
Mrinalini M. Rahatgaonkar

<p class="abstract">Rhabdomyosarcoma (RMS), a tumour of skeletal muscle origin, is the most common soft tissue sarcoma encountered in childhood. The head and neck region is the most common site of occurrence of RMS. RMS is a highly malignant tumour with extensive local invasions and early haemorrhagic and lymphatic dissemination. Despite the advances in treatment modalities, with aggressive approaches incorporating surgery, combination chemotherapy, and radiation therapy, the outcome for children with extensive, recurrent or metastatic disease remains poor. RMS in the head and neck region can be misdiagnosed as an infective or inflammatory swelling, thereby delaying the treatment. Here, we report a case of oral RMS in a 10-year-old child and highlight the need to include sinister pathologies like RMS in the differential diagnosis when dealing with cheek swellings in the paediatric age group.</p><p class="abstract"> </p>


Sign in / Sign up

Export Citation Format

Share Document