Results 131 to 140 of about 1,066 (165)
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Neural Fibrolipoma of the Foot
Journal of Computer Assisted Tomography, 2003Neural fibrolipoma is a benign tumor comprised of hypertrophied fibrofatty tissue with intermixed nerve tissue. We present the case of a neural fibrolipoma of the foot that underwent above-ankle amputation and review the characteristic features of this unique form of localized gigantism.
Justin Q, Ly +4 more
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Fibrolipoma of the nasopharynx
Saudi Journal of Otorhinolaryngology Head and Neck Surgery, 2020Nasopharyngeal fibrolipoma is exceedingly rare. This review article aims to recognize the characteristics of this rare tumor along with a favorable way to diagnose and treat it. We reviewed six cases of nasopharyngeal fibrolipoma. This lesion involves both sexes at any age.
MohammadH Shaheen, HebaZ Kufiah
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A Case of Tracheal Fibrolipoma
Acta Clinica Belgica, 1994We report the case of a tracheal fibrolipoma in a 40-year-old man successfully treated by laser photocoagulation. The clinical and pathological aspects, as well as the therapeutical options of this rare upper airway benign tumor are discussed.
F, Baharloo +5 more
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Fibrolipoma of the buccal mucosa
Oral Surgery, Oral Medicine, Oral Pathology, 1962Abstract A case of a fibrolipoma of the buccal mucosa has been reported, and a concept of origin of such tumors has been presented.
P D, TOTO, N, CHOUKAS
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The Journal of Foot and Ankle Surgery, 1999
Soft-tissue tumors of the toes are not particularly common; more tumors of the toes arise from the skin. The deeper tumors can be either benign or malignant and must be treated with caution until a histologic diagnosis has been made. However, malignant soft-tissue tumors of the toes are fairly rare.
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Soft-tissue tumors of the toes are not particularly common; more tumors of the toes arise from the skin. The deeper tumors can be either benign or malignant and must be treated with caution until a histologic diagnosis has been made. However, malignant soft-tissue tumors of the toes are fairly rare.
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The Journal of Dermatologic Surgery and Oncology, 1982
A case of a giant fibrolipoma dependent from the perineum and appearing like a second penis is described and illustrated in clinical and histologic aspects. Surgical ablation was accomplished easily and without incident.
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A case of a giant fibrolipoma dependent from the perineum and appearing like a second penis is described and illustrated in clinical and histologic aspects. Surgical ablation was accomplished easily and without incident.
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Fibrolipoma of the Median Nerve: An Overview
Current Rheumatology Reviews, 2022Imène Gharsallah, Maroua Slouma
exaly
Fibrolipoma of the tongue; a case report with literature review
Annals of Medicine and Surgery, 2021Abdulwahid Salih +2 more
exaly
Patologia polska, 1990
This report deals with a very uncommon benign testicular tumour, fibrolipoma. Orchidectomy was followed by the removal of the lymph nodes from the region of external iliac vessels. No recurrence appeared during 6-year follow-up.
B, Kuzaka, R, Pykało
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This report deals with a very uncommon benign testicular tumour, fibrolipoma. Orchidectomy was followed by the removal of the lymph nodes from the region of external iliac vessels. No recurrence appeared during 6-year follow-up.
B, Kuzaka, R, Pykało
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Laryngo- rhino- otologie, 2003
Benign mesenchymal tumors of the upper aerodigestive tract are very rare. In this localisation some tumors cause life-threatening upper airway obstruction. We report on a 42-year old man who complained dysphagia and globus sensation. The physical examination revealed a smooth tumor of the left aryepiglottic fold. A magnet resonance imaging (MRI) leaded
S, Grützenmacher +3 more
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Benign mesenchymal tumors of the upper aerodigestive tract are very rare. In this localisation some tumors cause life-threatening upper airway obstruction. We report on a 42-year old man who complained dysphagia and globus sensation. The physical examination revealed a smooth tumor of the left aryepiglottic fold. A magnet resonance imaging (MRI) leaded
S, Grützenmacher +3 more
openaire +1 more source