scholarly journals Giant Verrucous Haemangioma with Linear Features — A Rare Entity and Successful Treatment with Complete Excision and Grafting

JMED Research ◽  
2016 ◽  
pp. 1-5
Author(s):  
Kanakapura Nanjundaswamy Shivaswamy ◽  
S Shanthakumar K Rashm ◽  
A L Shyamprasad ◽  
T K Sumathy ◽  
M Y Suparna
F1000Research ◽  
2016 ◽  
Vol 5 ◽  
pp. 2905 ◽  
Author(s):  
Sunil Munakomi ◽  
Pramod Chaudhary

Herein we report a rare case of a giant myopericytoma presenting in a 16-year-old girl as a slowly progressive swelling involving the scalp in the occipital region. It was managed by complete excision. Histological examination of the lesion revealed  spindle-shaped cells forming characteristic rosettes around the blood vessels, and positive staining with smooth muscle actin.


2010 ◽  
Vol 2010 ◽  
pp. 1-3 ◽  
Author(s):  
Mani Anand ◽  
Sanjay D. Deshmukh ◽  
Dilip P. Pande ◽  
Suresh Naik ◽  
Dhyaneshwari P. Ghadage

Entomophthoromycosis is a rare entity. We hereby report a case of entomophthoromycosis in a three-year-old Asian child who presented with a painless, nontender, rapidly increasing large swelling on the thigh of six months duration, which was initially misdiagnosed as a soft tissue tumor and resected. The cause of misleading diagnosis was rapid growth of the lesion in a short duration of time, indicating the possibility of a tumor. Histopathological examination revealed an inflammatory lesion with aseptate fungal hyphae and the characteristic Splendore-Hoeppli phenomenon. Microbiological examination identified the fungus as Basidiobolus ranarum. Complete excision of the lesion followed by antifungal therapy was associated with complete recovery. Entomophthoromycosis should be considered early when children from endemic areas present with unusual, rapid-growing lesions of the subcutaneous region. In order to emphasize tumor-like presentation of zygomycosis, we are presenting this case.


2019 ◽  
Vol 2019 (6) ◽  
Author(s):  
Belal S Abufkhaida ◽  
Barah K Alsalameh

Abstract Liposarcoma is the most common retroperitoneal sarcoma and mesenchymal tumor in the abdomen. Usually, it presents with vague symptoms due to its large size and slow growth at the time of diagnosis. Liposarcoma is associated with a high local recurrence rate according to its histology, size and growth rate. Up till now, surgical resection is the only effective treatment for primary and recurrent abdominal liposarcoma. Secondary mesenteric liposarcoma is an extremely rare entity and so far a small number of cases have been reported in the literature. In this article, we present a rare case of a 63-year-old female patient who was diagnosed with mesenteric liposarcoma after 3 years of complete excision of retroperitoneal liposarcoma, presenting primarily as abdominal mass causing mechanical intestinal obstruction.


2014 ◽  
Vol 25 (4) ◽  
pp. 424-425 ◽  
Author(s):  
Zahide Simsek ◽  
Baris Yilmaz ◽  
Bora Aktas ◽  
Ata Turker Arikok ◽  
Sahin Coban

Neurosurgery ◽  
2004 ◽  
Vol 55 (4) ◽  
pp. E1001-E1005 ◽  
Author(s):  
A Alex Mohit ◽  
Joseph Eskridge ◽  
Richard Ellenbogen ◽  
Christopher I. Shaffrey

Abstract OBJECTIVE AND IMPORTANCE: Aneurysmal bone cysts (ABCs) are benign and expansile osteolytic lesions that can occur in any location in the spine, including the craniovertebral junction. Aggressive resection followed by bone grafting has been the mainstay of treatment, with selective arterial embolization as a presurgical adjunct. Complete excision of these lesions at the craniovertebral junction is associated with high surgical morbidity. We report a case of successful treatment of an ABC of the atlas in a child with selective arterial embolization alone. CLINICAL PRESENTATION: A 10-year-old girl presented with persistent neck pain after a snowboarding accident. Computed tomography and magnetic resonance imaging of the cervical spine revealed an expansile cystic mass involving the right lateral mass of C1. Digital subtraction angiography revealed a tumor blush, which, along with the cystic appearance of the lesion, was consistent with an ABC. INTERVENTION: The arterial feeders to the lesion were selectively embolized with polyvinyl alcohol particles. Three sessions of embolization were required to eradicate the blood supply to the lesion completely. CONCLUSION: Complete surgical resection of ABCs at the craniovertebral junction can be associated with high morbidity secondary to the highly vascular and destructive nature of these lesions. The case discussed here demonstrates the viability of selective arterial embolization as a primary and stand-alone modality of treatment.


2017 ◽  
Vol 18 (3) ◽  
pp. 217
Author(s):  
Bhumika Shivaram ◽  
AshaGowrappala Shanmukhappa ◽  
Leelavathy Budamakuntala ◽  
Archana Samynathan

Author(s):  
Shashikant A. Pol ◽  
Arjun Dass ◽  
Nitin Gupta ◽  
Aditi Mahajan

<p class="abstract">Antrochoanal polyp is a benign lesion, originating from the mucosa of the maxillary sinus, grow into maxillary sinus, nasal cavity and posteriorly to involve the choana. Nasal obstruction and nasal discharge are their main symptoms. Epistaxis is rare as seen in infected cases. Clinical assessment along with radiology helps in the diagnosis of antrochoanal polyp. We hereby describe a case of infected antrochoanal polyp in a 20-year-old female who presented with unilateral nasal obstruction, nasal discharge and intermittent epistaxis. Complete excision was done through endoscopic approach. On histopathology it showed secondary infection caused by actinomycosis which is extremely rare finding. This might be the first case report of actinomycosis infection in antrochoanal polyp as it was not found previously in any antrochoanal polyp case. Patient was followed till 6 month without any symptom.</p>


2018 ◽  
Vol 1 (Supplement) ◽  
pp. 61
Author(s):  
Şt. Cristea ◽  
R. Popescu ◽  
Şt. Cuculici ◽  
M. Sava ◽  
R. Vișan ◽  
...  

Abstract The partial or complete excision of the hemipelvis with the sparing of the lower limb is an option of the treatment of pelvic chondrosarcomas and a therapeutic alternative of the interilio-abdominal disarticulation. The operation has the same indications as the interilio-abdominal disarticulation and offers a good solution for avoiding a mutilating operation. A giant periacetabular pelvic chondrosarcoma developed in Ennequin zone II and partial zone III, was resected and reconstructed with iliofemoral cooptation after complex investigations - pelvic X-ray, CT, MRI, Bioptic confirmation. The wide excision of the tumor, a stable reconstruction, and an efficient recovery are essential for a successful treatment of pelvic chondrosarcomas.


2016 ◽  
Vol 13 (2) ◽  
pp. 92-93
Author(s):  
Anish M Singh ◽  
Janith L Singh ◽  
Bellu Kayastha ◽  
Prabin Shrestha

Brachial plexus schwannomas are rare benign nerve sheath tumors and only about 5% of schwannoma arise from the brachial plexus. They create a great challenge to surgeons due to their rare occurrence and complex anatomical location. We present a case of 37 yrs female presented with a right supraclavicular mass with severe radiating pain in right hand. Further investigation was done with MRI and FNAC which turns out to be huge right brachial plexus schwannoma. Gross total resection was done without any neurological motor defi cits. Nepal Journal of Neuroscience. Vol. 13, No. 2, 2016, Page: 92-93


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