scholarly journals Orbital Cystic Schwannoma Originating from the Frontal Nerve

2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
Yasuhiko Hayashi ◽  
Takuya Watanabe ◽  
Daisuke Kita ◽  
Yutaka Hayashi ◽  
Masayuki Takahira ◽  
...  

Schwannomas of the orbit are very rare benign neoplasms. Intraorbital cystic schwannomas originating from the frontal nerve are even rarer, with only 1 case reported to date. This is most likely due to the fact that, in most cases, the origin of the orbital schwannoma cannot be identified intraoperatively. The nerve origin is usually speculated from histological examination of the specimen and the postoperative neurological deficits of the patient. Here, we present the case of a 65-year-old woman with a one-month history of exophthalmos, whose orbital cystic lesion was completely removed by microsurgical transcranial operation. Intraoperatively, the continuity between the tumor and frontal nerve was seen macroscopically, leading us to confirm the frontal nerve as an origin of the tumor, which was consistent with the postoperative neurological findings. The diagnosis of the tumor was established as schwannoma from the histological examination. As a differential diagnosis of the orbital cystic lesions, the possibility of schwannomas should be kept in mind.

2015 ◽  
Vol 129 (10) ◽  
pp. 1036-1039 ◽  
Author(s):  
E Kyriakidou ◽  
T Howe ◽  
B Veale ◽  
S Atkins

AbstractBackground:Dermoid cysts in the floor of the mouth are relatively uncommon developmental lesions. They are thought to arise in the midline and along the lines of embryonic fusion of the facial processes containing ectodermal tissue.Case report:A 17-year-old female presented with a 3-month history of a growing, progressive swelling in the mouth floor. Clinical examination revealed a rather large symmetrical, soft swelling in the mouth floor, displacing the tongue superiorly. The fast growing nature and size of the lesion raised suspicion of potential compromise to the airway. Surgical excision was therefore performed.Conclusion:Differential diagnosis of cystic lesions in the floor of the mouth is of paramount importance, as the recommended surgical techniques vary depending on the anatomical position of the lesions. The intraoral approach is preferred for those lesions that do not extend beyond the mylohyoid muscle boundaries; this leads to a satisfactory cosmetic and functional outcome.


Author(s):  
Yassine Ouadnouni ◽  
Marouane Lakranbi ◽  
Mohamed Smahi

A 55 year old woman, presented to our hospital with a one year history of coughing and left chest pain. A chest CT-scan showed mediastinal, pleural and pulmonary cystic lesions evoking hydatidosis. Surgical exploration found a cystic lesion of the aorta-pulmonary window.


2020 ◽  
Vol 90 (3) ◽  
Author(s):  
Christos Kakos ◽  
Savvas Lampridis ◽  
Georgios Geropoulos ◽  
Reena Khiroya ◽  
Achilleas Antonopoulos ◽  
...  

Cystic fibrohistiocytic tumour of the lung is a very rare pathological entity that occurs either as a primary pulmonary neoplasm or as a metastasis from skin lesions called cellular fibrous histiocytomas. Herein, we present the case of a 19-year old man with a history of recurrent pneumothoraces who was managed surgically and was eventually diagnosed with cystic fibrohistiocytic tumour of the lung. Clinicians should include this disease in the differential diagnosis of pulmonary cystic lesions and be aware of its association with cellular fibrous histiocytoma. Reporting of more cases is warranted to further elucidate the natural course of the disease and optimise its management.


2013 ◽  
Vol 103 (2) ◽  
pp. 141-144 ◽  
Author(s):  
Mert Keskinbora ◽  
Özkan Köse ◽  
Yildirim Karslioglu ◽  
Bahtiyar Demiralp ◽  
Mustafa Basbozkurt

Benign fibrous histiocytoma is a rare benign primary skeletal tumor that occurs frequently in the long bones and the pelvis. The calcaneus is an unusual location for benign fibrous histiocytoma. We did not identify any case of benign fibrous histiocytoma involving the calcaneus in the relevant literature. We describe a 22-year-old male patient with benign fibrous histiocytoma involving the calcaneus treated with curettage and bone grafting. At the final follow-up visit, 1 year after surgery, the patient was free of pain and walking unaided. We discuss the differential diagnosis of cystic lesions of the calcaneus. (J Am Podiatr Med Assoc 103(2): 141–144, 2013)


2004 ◽  
Vol 132 (11-12) ◽  
pp. 435-437
Author(s):  
Radoje Colovic ◽  
Nikica Grubor ◽  
Vladimir Radak ◽  
Natasa Colovic ◽  
Mirjana Stojkovic

Hydatid cyst of the pancreas is rare. During the last 30 years, less than 40 cases have been reported in journals on Medline. This is a case report of a 35-year old woman with 2-year history of epigastric pain in whom an ultrasound and computed tomography showed the cyst of the body and tail of the pancreas 6x7 cm in diameters, which was supposed to be hydatid one. During surgery, an isolated hydatid cyst of the pancreas was found without communication with the pancreatic duct. The content of the cyst was removed, and pericyst was partially excised and drained. The recovery was uneventful and the patient has remained symptom free so far. Although rare, hydatid cyst should be considered in the differential diagnosis of the cystic lesions of the pancreas, particularly in patients coming from endemic areas and without history of pancreatitis.


2021 ◽  
Vol 49 ◽  
Author(s):  
Giovanna Lapkoski Bonatto ◽  
Victoria Gariba E Silva ◽  
Lucas Jocemir Favero ◽  
Natália Noreika Kano ◽  
Renato Silva De Sousa ◽  
...  

Background: Feline mammary hyperplasia (FMH) is a benign disease that commonly affects young females, once it is caused by the exaggerated stimulation of endogenous or exogenous progestogen. FMH leads to acute edema and inflammation of the mammary glands and frequently evolve to ulcerations, secondary infections, and systemic clinical signs. Even though it is rare in male cats, progesterone therapy or an unknown endogenous source of hormone can cause the disease. This report aims to describe a case of FMH in a male feline with no history of hormonal treatment and treated with radical surgical resection. Case: A 7-month-old intact male domestic shorthair cat was presented due to acute onset of generalized mammary tumors which had progressed for 18 days. Tumors size had 5 cm large in diameter, symmetric, bilateral, and affected all mammary glands. The tissue was firm, hyperemic, and ulcerated. FMH was initially suspected but with a differential diagnosis for mammary adenocarcinoma. Except for pain on tumor palpation, there was no other clinical abnormality. Survey thoracic radiographs and abdominal ultrasound did not find signs of metastasis or hermaphroditism. Fine-needle aspirate biopsy and further cytological examination were inconclusive. Surgical resection through a single-stage bilateral total mastectomy and reconstruction using a left flank fold flap was elected. There were no intraoperative complications and the cat recovered well, with good healing and no clinical signs 21 days after the surgery. Histological examination of the mammary glands confirmed the diagnosis of FMH due to the non-neoplastic characteristics and tissue’s benign biological behavior. Eleven months after diagnosis, the cat was asymptomatic.Discussion: The FMH frequently affects young females and is associated with gestational periods, the end of the estrous cycle, and, most commonly, hormonal therapy with synthetic progesterone. Male cats are rarely affected with or without a history of progesterone administration, which is commonly used for treatment of dermatopathies, urinary incontinence, control of behavioral changes, or mistakenly as a contraceptive. Clinical signs are the acute onset of mammary tumors with firm consistency, inflammation, ulcerated areas, absence of mammary secretion, and mobility difficulty due to local swelling. Systemic clinical signs including apathy, anorexia, fever, and dehydration can occur. The main differential diagnosis is mammary neoplasia and diagnosis is suspected by the patient’s history, disease progression, and histological examination. Conservative treatment using a progesterone inhibitor, such as aglepristone, can be performed but usually take a few weeks to promote total remission, may require additional administration, and does not prevent a possible recurrence. Radical mastectomy is an alternative to late-stage disease. It was chosen toperform a single-stage bilateral mastectomy for surgical removal of the FMH in this case mainly considering that it was a male cat with no detectable progesterone source, marked swelling, and a clinical condition that could deteriorate quickly. The FMH prognosis is good when there are no secondary infections or systemic signs, making it possible to maintain quality of life after treatment. The FMH must be considered a differential diagnosis for feline mammary tumors, regardless of gender and history of progesterone administration.


2022 ◽  
pp. 014556132110725
Author(s):  
Rui Lu ◽  
Xiong Chen ◽  
Shucheng Yin ◽  
Zhiyong Li

Lipomas of the palatine tonsil are rare benign neoplasms in clinical practice. We present a case of palatine tonsillar fibroangiolipoma in a 50-year-old Chinese male with a history of multiple lipomas on the back and extremities. It was diagnosed based on histological examination and integrated analysis. Good wound healing and no evidence of recurrence were noted within 6 months follow-up after tonsillectomy. This article also puts a spotlight on the differential diagnosis of benign tonsillar tumors and reviewed recent relevant literature.


2019 ◽  
Vol 98 (5) ◽  
pp. E21-E23
Author(s):  
Evelyne S. Diom ◽  
Johannes J. Fagan ◽  
Ellen Bolding

Objective: We report a rare case of an intralingual ranula. The differential diagnosis, etiology, diagnostic features, and management are discussed. Case Report: An 18-year-old man presented with a mass that extended along the ventral surface of the tongue and up to the tip. The computed tomography scan clearly defined the extent of a cystic lesion. The pathologic diagnosis of an intralingual ranula was made. Conclusion: Lingual cysts have a varied etiology. Diagnosis hinges on histological examination of the cyst wall. Conservative resection and histological examination is the standard of care.


2018 ◽  
Vol 27 (3) ◽  
pp. 297-300 ◽  
Author(s):  
Rabea A. Gadelkareem ◽  
Ayman A. Elqady ◽  
Sayed K. Abd-Elshafy ◽  
Hisham Imam ◽  
Hassan A. Abolella

Objective: The aim of this work is the presentation of a case of isolated renal hydatid cyst with novel findings and an unusual surgical scenario. Clinical Presentation and Intervention: A 54-year-old female patient presented with left loin pain and a palpable left renal mass. Imaging described a well-demarcated left renal cystic lesion with a double-layer wall. Radical nephrectomy was performed due to the possibility of malignancy. On retrograde revision, the double-layer wall represented the detached germinative membrane of a hydatid cyst that was confirmed by histopathology. Conclusion: Isolated renal hydatid cyst could be misinterpreted as a renal tumor. It should be considered in the differential diagnosis of renal cystic lesions.


2015 ◽  
Vol 7 (1) ◽  
pp. 75-78 ◽  
Author(s):  
Jia Li Liau ◽  
Davide Altamura ◽  
Marzena Ratynska ◽  
Roberto Verdolini

Malignant degeneration within epidermal cysts is very rare. However, these lesions may not be recognised clinically, and histological examination plays an important role in arriving at a correct diagnosis. Hence, we believe that benign-looking cystic lesions with a history of progressive growth should be surgically excised and submitted for histopathological assessment.


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