scholarly journals Nevus lipomatosus cutaneous superficialis presenting as papilloma: A case report

2021 ◽  
Vol 7 (4) ◽  
pp. 367-369
Author(s):  
Shagufta Tahir Mufti ◽  
Shreya Mehdiratta ◽  
Salim Tahir ◽  
M.M.A. Faridi
Keyword(s):  
Adipose Tissue ◽  
Rare Case ◽  
Soft Tissue Mass ◽  
Histopathological Examination ◽  
Review Of Literature ◽  
Tissue Mass ◽  
Dermal Collagen ◽  
History Of ◽  
Smooth Skin ◽  
The Right

Nevus Lipomatosus Cutaneous Superficialis (NLCS) is an uncommon hamartomatous lesion of the skin. NLCS is classified into two clinical forms classic and solitary. Some authors consider this lesion as a type of connective tissue nevus. We report a rare case of solitary NLCS in a 69 year old male with a long history of pedunculated swelling in the right gluteal cleft with review of literature. On gross appearance the lesion was a grey brown, exophytic, cerebriform, smooth skin covered soft tissue mass measuring 4.5 cms in the largest dimension with a broad peduncle attached. On histopathological examination the lesion showed superficial and deep dermal infiltration of the adipose tissue with distortion of the dermal collagen.

scholarly journals Lágyéksérvet utánzó gigantikus méretű myxoid leiomyoma

2016 ◽  
Vol 157 (10) ◽  
pp. 392-395
Author(s):  
Orsolya Huszár ◽  
Attila Zaránd ◽  
Gyöngyi Szántó ◽  
Viktória Juhász ◽  
Eszter Székely ◽  
...  
Keyword(s):  
Quality Of Life ◽  
Smooth Muscle ◽  
Soft Tissue Mass ◽  
Smooth Muscle Tumour ◽  
Tissue Mass ◽  
Abdominal Symptoms ◽  
History Of ◽  
The Right

Leiomyoma is a rare, smooth muscle tumour that can occur everywhere in the human body. The authors present the history of a 60-year-old female, who had a giant, Mullerian type myxoid leiomyoma in the inguinal region mimicking acute abdominal symptoms. After examination the authors removed the soft tissue mass in the right femoral region reaching down in supine position to the middle third of the leg measuring 335 × 495 × 437 mm in greatest diameters in weight 33 kg. Reconstruction of the tissue defect was performed using oncoplastic guidelines. During the follow-up time no tumour recurrence was detected and the quality of life of the patient improved significantly. Orv. Hetil., 2016, 157(10), 392–395.

scholarly journals Aggressive angiomyxoma of broad ligament: an uncommon mesenchymal tumor

2019 ◽  
Vol 8 (7) ◽  
pp. 2913
Author(s):  
Sunil Vitthalrao Jagtap ◽  
Nitesh Nasre ◽  
Nitin S. Kshirsagar ◽  
Shubham S. Jagtap
Keyword(s):  
Soft Tissue Mass ◽  
Histopathological Examination ◽  
Broad Ligament ◽  
Mesenchymal Tumor ◽  
Aggressive Angiomyxoma ◽  
Recurrent Pain ◽  
Lower Abdomen ◽  
Radiological Findings ◽  
Tissue Mass ◽  
History Of

Aggressive angiomyxoma is a rare mesenchymal tumor occurring predominantly in the pelviperineal region. Authors present a case of a 70 years female presented with history of distention of lower abdomen with recurrent pain since 6 months. On clinical examination there was suspicion of fibroid. On USG it was reported as huge fleshy, soft tissue mass measuring 20x10x9 cm in lower abdominal flanks and pelvis with vascular pedicle attached to right parametrium. Pan-hysterectomy was performed. Right broad ligament showed mass measuring 18.5x10x6 cm. On histopathological examination it was diagnosed as a case of Aggressive angiomyxoma of broad ligament. We are presenting this case for its extreme rarity, clinicohisto-pathological and radiological findings.

Organised haematoma of the sphenoid sinus mimicking a pituitary tumour

2009 ◽  
Vol 124 (1) ◽  
pp. 83-85 ◽  
Author(s):  
T Nakagawa ◽  
Y Kawai ◽  
T Sakamoto ◽  
J Ito
Keyword(s):  
Differential Diagnosis ◽  
Sphenoid Sinus ◽  
Rare Case ◽  
Soft Tissue Mass ◽  
Histopathological Examination ◽  
Sella Turcica ◽  
Pituitary Tumour ◽  
Tissue Mass ◽  
Bony Destruction ◽  
Complete Surgical Resection

AbstractObjective:We report an extremely rare case of an organised haematoma arising in the sphenoid sinus.Case report:An 85-year-old woman presented with an expansile soft tissue mass in the left sphenoid sinus, with bony destruction of the sella turcica, which mimicked the extrasellar extension of a pituitary tumour. The tumour was excised using an endoscopic, transsphenoidal approach. Histopathological examination revealed an organised haematoma.Conclusion:To our knowledge, this is the first report of an organised haematoma arising in the sphenoid sinus. This case indicates that organised haematoma should be included in the differential diagnosis of extensive sphenoid lesions; it also emphasises the importance of correct pre-operative diagnosis for therapeutic planning, as complete surgical resection by an endoscopic approach is curative.

Isolated tubercular hypoglossal nerve paralysis

2016 ◽  
Vol 47 (3) ◽  
pp. 255-260 ◽  
Author(s):  
JS Thakur ◽  
Naina Verma ◽  
Shobha Mohindroo ◽  
Ramesh K Azad ◽  
NK Mohindroo
Keyword(s):  
Nerve Palsy ◽  
Hypoglossal Nerve ◽  
Soft Tissue Mass ◽  
Histopathological Examination ◽  
Posterior Wall ◽  
Tissue Mass ◽  
Nerve Paralysis ◽  
Hypoglossal Nerve Palsy ◽  
Neurological Finding ◽  
The Right

Hypoglossal nerve palsy is not an uncommon neurological finding but primary nasopharyngeal tuberculosis (TB) presenting as hypoglossal nerve palsy is very rare. A 31-year-old woman presented with headache and progressive tongue deviation towards the right side. Diagnostic nasal endoscopy revealed soft tissue mass lesion on the posterior wall of nasopharynx while MRI revealed isointense tumour in nasopharynx with normal hypoglossal nerve and brain. Histopathological examination found TB. We discuss the clinical challenges and possible pathogenesis of this rare clinical entity.

scholarly journals Primary Chordoma of the Nasopharynx: A Rare Case Report and Review of the Literatures

2019 ◽  
Vol 2019 ◽  
pp. 1-6 ◽  
Author(s):  
Ery Kus Dwianingsih ◽  
Yosinta Snak ◽  
Hanggoro Tri Rinonce ◽  
Brian Wasita ◽  
Ester Lianawati Antoro ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Rare Case ◽  
Soft Tissue Mass ◽  
Histopathological Examination ◽  
Axial Skeleton ◽  
Cystic Mass ◽  
Radiological Imaging ◽  
Tissue Mass ◽  
Rare Case Report ◽  
Nasopharyngeal Mass

Primary chordoma of the nasopharynx is an extremely rare malignant tumor of notochordal origin in the extra-osseous axial skeleton. It presents as a soft tissue mass without involvement of the skull base bone (clivus) and may mimic other lesions of the nasopharynx. A 26-year-old male patient is presented with nasal obstruction and congestion for the last 3 years. Physical and radiological examination revealed a mass in the naso-oropharyngeal region. It was suspected to be a cystic mass or abscess on radiological imaging. However, histopathological examination revealed a chordoma. We review all 20 cases of primary nasopharyngeal chordoma reported previously in the literature. Nasopharyngeal chordoma should be considered in the differential diagnosis of nasopharyngeal mass due to its unspecific appearance on clinical and radiology examination.

Primary vesical actinomycosis with changes of cystitis cystica presenting as bladder mass

2021 ◽  
Vol 0 ◽  
pp. 1-4
Author(s):  
Nagendra Mishra ◽  
Henil Upadhyay ◽  
Charmy Parikh
Keyword(s):  
Soft Tissue ◽  
Urinary Bladder ◽  
Soft Tissue Mass ◽  
Histopathological Examination ◽  
Bladder Wall ◽  
Tissue Mass ◽  
Rare Differential Diagnosis ◽  
The Right ◽  
Cystitis Cystica ◽  
Bladder Mass

Actinomycosis is a rare chronic granulomatous suppurative infection caused by Gram-positive bacteria. The occurrence of primary vesical actinomycosis is extremely rare and only a few cases have been reported. Pre-operative diagnosis of vesical actinomycosis is challenging as the clinical and radiological features usually point towards bladder malignancy. Therefore, in most cases, definitive diagnosis is usually made after histopathological examination of the involved tissue. A 60-year-old male presented with complaints of hematuria, burning micturition, irritative, and obstructive urinary symptoms for 15 days. USG revealed a large soft-tissue mass having a polypoidal intraluminal and extraluminal component and involving the right posterolateral urinary bladder wall. CT scan showed a large irregular soft-tissue mass with multiple cystic lesions involving the right lateral wall of the urinary bladder. Transurethral resection of bladder mass biopsy was performed and the histopathological examination showed bacterial colonies of Actinomyces with changes of cystitis cystica. The patient was treated with amoxicillin and potassium clavulanate for 3 months. Actinomycosis should be kept as a rare differential diagnosis in cases presenting as bladder mass. The diagnosis is most commonly made by histopathology and may need a repeat biopsy to arrive at the correct diagnosis. The patient should be treated by penicillin group of antibiotics for 2–3 months and followed up for years to detect any recurrence.

scholarly journals Ocular Inflammatory Myofibroblastic Tumor in the Left Eye with Phthisis Right Eye: A Rare Occurrence in a Child

2015 ◽  
Vol 2015 ◽  
pp. 1-5 ◽  
Author(s):  
Sangeeta Shah ◽  
Badri Prasad Badhu ◽  
Poonam Lavaju ◽  
Anju Pradhan
Keyword(s):  
Inflammatory Myofibroblastic Tumor ◽  
Soft Tissue Mass ◽  
Histopathological Examination ◽  
Rare Occurrence ◽  
Medial Canthus ◽  
Local Growth ◽  
Anterior Portion ◽  
Tissue Mass ◽  
Lateral Canthus ◽  
The Right

Inflammatory myofibroblastic tumor (IMT) is a benign pseudoneoplastic inflammatory condition with the potential for persistent local growth and recurrence that rarely affects the orbit. We report a very rare case of anterior orbital IMT in a child who presented with gradually progressive mass in left eye for 16 months. Ocular examination showed a cauliflower like exophytic mass at 360 degrees of the perilimbal area covering the entire cornea and obscuring the visualization of anterior and posterior segments. The right eye was phthisical. CT scan showed a lobulated exophytic soft tissue mass in the preseptal region and along the anterior portion of the left globe extending from medial canthus to the lateral canthus. Enucleation of the left eye was performed and the histopathological examination confirmed the diagnosis of IMT. This report aims to raise awareness about this rare ocular entity and emphasizes its early treatment as delay can result in loss of the eye.

Popliteal artery thrombosis secondary to a tibial osteochondroma

VASA ◽  
2011 ◽  
Vol 40 (3) ◽  
pp. 251-255 ◽  
Author(s):  
Gruber-Szydlo ◽  
Poreba ◽  
Belowska-Bien ◽  
Derkacz ◽  
Badowski ◽  
...  
Keyword(s):  
Case Report ◽  
Magnetic Resonance Angiography ◽  
Popliteal Artery ◽  
Doppler Ultrasonography ◽  
Histopathological Examination ◽  
Previous History ◽  
Plain Radiography ◽  
Artery Thrombosis ◽  
History Of ◽  
The Right

Popliteal artery thrombosis may present as a complication of an osteochondroma located in the vicinity of the knee joint. This is a case report of a 26-year-old man with symptoms of the right lower extremity ischaemia without a previous history of vascular disease or trauma. Plain radiography, magnetic resonance angiography and Doppler ultrasonography documented the presence of an osteochondrous structure of the proximal tibial metaphysis, which displaced and compressed the popliteal artery, causing its occlusion due to intraluminal thrombosis..The patient was operated and histopathological examination confirmed the diagnosis of osteochondroma.

scholarly journals Thymoma in an aged backyard Leghorn chicken, with reviews of a database and literature

2021 ◽  
Vol 33 (2) ◽  
pp. 336-339
Author(s):  
Julia Blakey ◽  
Carmen Jerry ◽  
Ana da Silva ◽  
Simone Stoute
Keyword(s):  
Soft Tissue Mass ◽  
Animal Health ◽  
Postmortem Examination ◽  
Cervical Region ◽  
Laboratory System ◽  
Unexpected Death ◽  
Tissue Mass ◽  
Microscopic Features ◽  
History Of ◽  
Backyard Chickens

A 7-y-old backyard Leghorn chicken ( Gallus domesticus) was submitted to the California Animal Health and Food Safety Laboratory System (CAHFS)–Turlock branch for postmortem examination, with a history of unexpected death. At postmortem examination, a hemorrhagic soft tissue mass was observed in the cervical region. Microscopically, a densely cellular neoplasm of polygonal epithelial cells and small lymphocytes was observed. The microscopic features of the neoplasm in combination with positive immunohistochemistry for pancytokeratin and CD3 were used to classify the lesion as a thymoma. Thymoma was diagnosed in only 5 birds submitted to CAHFS from 1990 to 2019. Thymoma has been described only rarely in birds, and is an unusual diagnosis in backyard chickens.

A RARE CASE OF HETEROTOPIC PANCREATIC TISSUE CAUSING SMALL BOWEL OBSTRUCTION

2021 ◽  
pp. 4-5
Author(s):  
B. Santhi ◽  
M. Annapoorani ◽  
Sharada bhavana
Keyword(s):  
Intestinal Obstruction ◽  
Rare Case ◽  
Histopathological Examination ◽  
Pancreatic Tissue ◽  
Acute Intestinal Obstruction ◽  
Emergency Laparotomy ◽  
Review Of Literature ◽  
Heterotopic Pancreatic Tissue ◽  
Small Growth ◽  
Upper Gastrointestinal

A Rare case of heterotopic pancreatic tissue of ileum causing acute intestinal obstruction has been described with a brief review of literature. A 42 yr old male patient presented to the emergency department with features of acute intestinal obstruction. After evaluation patient was taken up for emergency laparotomy which revealed a band to be arising from ileum. Furthermore, there was a small growth in the ileal wall at the site of origin of the band. Hence resection of the growth was done and followed by ileoileal anastomosis. Later on, histopathological examination of the growth revealed it to be heterotopic pancreatic tissue. Heterotopic pancreatic tissue is often an incidental nding encountered in upper gastrointestinal tract during endoscopy and surgeries. But Symptomatic ectopic pancreas of ileum is relatively rare and they very rarely present with acute symptoms as in this case

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