scholarly journals Spindle Cell Lipoma of Scrotum

2019 ◽  
Vol 2 (2) ◽  
pp. e40-e41
Author(s):  
Muhammad Iqbal ◽  
Sanjay Agarwal ◽  
Iqbal S. Shergill
Keyword(s):  
Male Patient ◽  
Spindle Cell ◽  
Benign Lesion ◽  
Histopathological Diagnosis ◽  
Spindle Cell Lipoma ◽  
Rare Presentation ◽  
Left Half

Spindle cell lipoma (SCL) in the scrotum is a very rare presentation with only a few cases reported in the literature. The most common sites for this benign lesion are the neck, shoulder, and back. We present a 72-year-old male patient with painless swelling on the left half of the scrotum with a histopathological diagnosis of SCL.

scholarly journals Left Supraclavicular Spindle Cell Lipoma

2010 ◽  
Vol 2010 ◽  
pp. 1-4 ◽  
Author(s):  
Oladejo Olaleye ◽  
Bertram Fu ◽  
Ram Moorthy ◽  
Charles Lawson ◽  
Myles Black ◽  
...  
Keyword(s):  
Spindle Cell ◽  
Excisional Biopsy ◽  
Neurological Deficits ◽  
Excision Biopsy ◽  
Low Grade ◽  
Spindle Cell Lipoma ◽  
Rare Presentation ◽  
Spindle Cells ◽  
Immuno Histochemistry ◽  
Rare Benign Tumour

Background. Spindle cell lipoma (SCL) is a benign lipomatous tumour, typically occurring in the posterior neck, shoulder or upper back of elderly males. They compose of fat, CD34 positive spindle cells, and ropey collagen on a myxoid matrix. This case highlights a rare presentation of SCL and the need for pre-operative diagnosis.Case Report. A 63-year-old gentleman presented with a pre-existing left supraclavicular mass that had recently increased in size. FNA and CT Scans were performed and results discussed in the mutidisciplinary team meeting. Excisional biopsy was recommended.Radiology. CT neck showed a left supraclavicular mass of fatty density with fine internal septations. A low-grade liposarcoma could not be excluded.Histopathology. FNA was indeterminate. Histology of specimen showed bland spindle cells with no evidence of malignancy. Immuno-histochemistry showed SCL with CD34 positivity and negative staining on CDK4 and p16.Management. Excision biopsy of the mass was performed which was technically difficult as the mass invaginated around the brachial plexus. The patient recovered well post-operatively with no neurological deficits.Conclusion. Spindle cell lipoma is a rare benign tumour and a pre-operative diagnosis based on the clinical context, imaging and immuno-histochemistry is crucial to management.

scholarly journals Pleomorphic lipoma: A rare entity

2021 ◽  
Vol 8 (4) ◽  
pp. 515-517
Author(s):  
Goutami Das Nayak ◽  
Shushruta Mohanty ◽  
Meenakshi Mohapatro
Keyword(s):  
Spindle Cell ◽  
Histopathological Diagnosis ◽  
Spindle Cell Lipoma ◽  
Soft Tissue Tumours ◽  
Pleomorphic Lipoma ◽  
Atypical Cells ◽  
Posterior Neck ◽  
Subcutaneous Mass ◽  
Slow Growing ◽  
Malignant Soft Tissue

Pleomorphic lipoma is a rare neoplasm that is considered as a variant of spindle cell lipoma. It predominantly occurs in the dermis or subcutis of the posterior neck, upper back, and shoulders. Pleomorphic lipoma may clinically present as a slow-growing and well-circumscribed subcutaneous mass. Though it is a benign tumour it may contain atypical cells for which it may mimick sarcoma or other malignant soft tissue tumours. So histopathological diagnosis is vital for preventing unnecessary surgery. Here we report a case of a pleomorphic lipoma on upper back in a 55yr old patient.

Intramuscular spindle cell lipoma of the sternomastoid muscle – imaging and pathological appearances

2006 ◽  
Vol 6 (1) ◽  
pp. 43-45 ◽  
Author(s):  
M. D. Williams ◽  
D. C. Howlett ◽  
N. Violaris ◽  
K. Ramesar
Keyword(s):  
Skeletal Muscle ◽  
Differential Diagnosis ◽  
Magnetic Resonance ◽  
Mr Imaging ◽  
Male Patient ◽  
Spindle Cell ◽  
Imaging Features ◽  
Spindle Cell Lipoma ◽  
Sternomastoid Muscle ◽  
Male Patients

Spindle cell lipoma (SCL) is a rare neoplasm occurring predominantly in male patients between the ages of 45 and 70 years. We present a case of SCL arising in the sternomastoid muscle of a 46 year old male patient, which was completely excised at surgery. (Only 4 cases of SCL have been described within skeletal muscle and SCL has not previously been reported within sternomastoid.) The histological and magnetic resonance (MR) imaging features of this lesion are described and the differential diagnosis is discussed, with particular reference to its potential confusion with liposarcoma.

scholarly journals Primary Pulmonary Synovial Sarcoma: A Very Rare Presentation

2014 ◽  
Vol 2014 ◽  
pp. 1-3
Author(s):  
Ekrem Cengiz Seyhan ◽  
Sinem Nedime Sokucu ◽  
Gulsah Gunluoglu ◽  
Nurdan Simsek Veske ◽  
Sedat Altin
Keyword(s):  
Synovial Sarcoma ◽  
Epithelial Membrane Antigen ◽  
Spindle Cell ◽  
Lower Lobe ◽  
Soft Tissue Sarcomas ◽  
Histopathological Diagnosis ◽  
Rare Presentation ◽  
Mesenchymal Tissue ◽  
Thorax Ct ◽  
Primary Pulmonary Synovial Sarcoma

Synovial sarcoma (SS) is a rare tumor originating from mesenchymal tissue and accounting for approximately 5–10% of all soft tissue sarcomas. A rare case of primary pulmonary SS in an asymptomatic 18-year-old man admitted to our hospital for investigation of a 6 × 6.5 cm, oval-shaped, well-delineated pleural based peripheral mass in the left lower lobe in his thorax CT is presented. Left lower lobectomy was done. Immunohistochemically, tumor cells were positive for cytokeratin, epithelial membrane antigen (EMA), and vimentin so that the histopathological diagnosis was compatible with biphasic spindle cell type SS in the lung.

scholarly journals Intramuscular spindle cell lipoma/pleomorphic lipoma unusual site fore arm

2018 ◽  
Vol 6 (4) ◽  
pp. 1459
Author(s):  
Anu Anna Jacob ◽  
Geethanjali N. ◽  
Usha Poothiode
Keyword(s):  
Fine Needle Aspiration ◽  
Fine Needle Aspiration Biopsy ◽  
Spindle Cell ◽  
Subcutaneous Tissue ◽  
Needle Aspiration ◽  
Spindle Cell Lipoma ◽  
Rare Presentation ◽  
Unusual Site ◽  
Fine Needle ◽  
Pleomorphic Lipoma

Pleomorphic lipoma/ spindle cell lipoma accounts for 15 % of lipoma within extremities, confining to the superficial plain comprising lower dermis and subcutaneous tissue. Intramuscular presentation in extrimities is a rare presentation. Here is a case of deep seated pleomorphic lipoma, of forearm, both on fine needle aspiration, biopsy and IHC confirmation. 100% of benign cases of lipoma are positive for CD 34, as stated in many studies and was also positive in our case.

Intrathoracic Myxoid Spindle Cell Lipoma: A Rare Presentation of a Myxoid Neoplasm

2020 ◽  
Vol 109 (5) ◽  
pp. e343-e345
Author(s):  
Steven P. Schulberg ◽  
Derek Lim ◽  
Syed T. Hoda ◽  
Mikhail Vaynblat
Keyword(s):  
Spindle Cell ◽  
Spindle Cell Lipoma ◽  
Rare Presentation

scholarly journals Exceptionally large, atypically located spindle cell lipoma

2019 ◽  
Vol 12 (10) ◽  
pp. e232209
Author(s):  
Mitchell John ◽  
Shaan Patel ◽  
George Joseph
Keyword(s):  
Spindle Cell ◽  
Excisional Biopsy ◽  
Large Mass ◽  
Spindle Cell Lipoma ◽  
Rare Presentation ◽  
Spindle Cells ◽  
Histological Appearance ◽  
Bony Involvement ◽  
Immunohistological Analysis ◽  
Rule Out

Spindle cell lipomas are a rare subtype of lipoma typically occurring in the shawl region of middle-aged men with a characteristic histological appearance consisting of mature adipocytes, ropey collagen and spindle cells. Those of extraordinary size or atypical anatomic location require a proper immunohistological workup to rule out more ominous malignancy. The authors report the rare presentation of a 54-year-old man with a large mass of the left palm causing discomfort and paresthesia for 6 months. Radiographs showed a radiolucent mass without mineralisation or bony involvement. MRI demonstrated a non-contrast-enhancing homogeneous lipomatous mass encompassing flexor tendons of the palm. Elective excisional biopsy and immunohistological analysis were consistent with spindle cell lipoma measuring 11 cm × 7 cm × 4 cm. This case is the largest spindle cell lipoma of the hand reported in the literature and appears to be the largest described in the upper extremity.

Spindle Cell Lipoma of the Posterior Axilla: A Case Report

2008 ◽  
Vol 59 (1) ◽  
pp. 45
Author(s):  
Jee Young Lee ◽  
Kyung Jin Suh ◽  
Sang Yoon Kim
Keyword(s):  
Case Report ◽  
Spindle Cell ◽  
Spindle Cell Lipoma

SPINDLE CELL LIPOMA MASQUERADING AS MIXED PYOLARYNGOCELE : A RARE CASE REPORT

2020 ◽  
Vol VOLUME 8 (ISSUE 1) ◽  
pp. 47-51
Author(s):  
Vineet Narula
Keyword(s):  
Rare Case ◽  
Spindle Cell ◽  
Spindle Cell Lipoma ◽  
Computed Tomographic ◽  
Contrast Enhanced ◽  
Rare Case Report ◽  
Shoulder Region ◽  
Cervical Approach ◽  
Posterior Neck ◽  
Keywords Lipoma

ABSTRACT Spindle Cell Lipoma (SCL) is an uncommon benign tumor of adipose tissue that is usually super􀃶cially located in the posterior neck, back and shoulder region. We report a rare case of SCL in a 39 years old male presenting as neck swelling with c/o stridor and dysphagia. The contrast enhanced computed tomographic scan of neck showed an external and internal part of the swelling traversing through the thyrohyoid membrane suggestive of Mixed Pyolaryngocele. The tumor was excised by a trans-cervical approach but the post operative histopathology was found to be spindle cell Lipoma. We report this case due to its atypical presentation and location. Keywords: Lipoma, Spindle cell, Pyolaryngocele

scholarly journals Concurrent Inverted Papilloma and Squamous Cell Carcinoma with Intradural Extension Presenting with Frontal Lobe Syndrome

2021 ◽  
Author(s):  
Abdul Jaleel ◽  
Pavithran V. M. ◽  
Shanavas Cholakkal ◽  
Vineeth Kadangot Kuthampulli
Keyword(s):  
Squamous Cell Carcinoma ◽  
Cell Carcinoma ◽  
Frontal Lobe ◽  
Squamous Cell ◽  
Benign Lesion ◽  
Lateral Wall ◽  
Inverted Papilloma ◽  
Intracranial Extension ◽  
Rare Presentation ◽  
Frontal Lobe Syndrome

Abstract Inverted papilloma is an uncommon tumor mostly arising from the lateral wall of the nasal cavity and displays a benign but locally aggressive behavior. Intracranial extension is an extremely rare presentation of inverted papilloma. Extension occurs either as a benign lesion or due to malignant transformation. We report a case of concurrent inverted papilloma and squamous cell carcinoma presenting with epistaxis and recent-onset altered behavior and memory impairment. After literature review of similar cases having inverted papilloma with intracranial extension, we could identify a total of 12 cases, most of which were recurrences of a primary inverted papilloma that were resected before extension into the cranial cavity. Most cases were of extradural extension, and intradural spread resulted in poor prognosis on follow-up. Concurrent inverted papilloma and squamous cell carcinoma extending into the anterior cranial fossa and frontal lobe is a very rare clinical entity and can present as frontal lobe syndrome.

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