Results 181 to 190 of about 41,692 (236)
Intratendinous Lipoma of Biceps Long Head: A Case Report and Current Concepts Review of Musculoskeletal Lipomas. [PDF]
J Orthop Case RepArunachalam AK +3 more
europepmc +1 more source
Efficacy and safety of CBL-514 for Dercum disease lipomas: A randomized phase 2a study. [PDF]
JAAD IntHerbst KL +4 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
The Thoracic and Cardiovascular Surgeon, 1988
The endobronchial lipoma is one of the rarest tumours of the tracheobronchial tree. They are histologically benign tumours. But, they can produce pulmonary damage or irreversible bronchiectasis if diagnosis and treatment are delayed. The treatment of choice in most cases is bronchoscopic removal.
R, Doğan +3 more
openaire +2 more sources
The endobronchial lipoma is one of the rarest tumours of the tracheobronchial tree. They are histologically benign tumours. But, they can produce pulmonary damage or irreversible bronchiectasis if diagnosis and treatment are delayed. The treatment of choice in most cases is bronchoscopic removal.
R, Doğan +3 more
openaire +2 more sources
Neuropediatrics, 1992
Intracranial lipomas are very rare tumors, mostly being localized in the midline and often asymptomatic. We report on three children with intracranial lipomas (one with extension to the cervical spinal cord) diagnosed by CT and/or MR. All three had different symptoms and neurological signs.
F, Donati +3 more
openaire +2 more sources
Intracranial lipomas are very rare tumors, mostly being localized in the midline and often asymptomatic. We report on three children with intracranial lipomas (one with extension to the cervical spinal cord) diagnosed by CT and/or MR. All three had different symptoms and neurological signs.
F, Donati +3 more
openaire +2 more sources
Acta Neurochirurgica, 1991
Intracranial lipomas are very rare, probably congenital lesions. Though they can occur anywhere in the intracranial space, a good proportion of cases tend to be located around the midline. Review of the literature as well as our own three cases--which forms the basis of this article--shows that they are mostly asymptomatic.
P O, Eghwrudjakpor +3 more
openaire +2 more sources
Intracranial lipomas are very rare, probably congenital lesions. Though they can occur anywhere in the intracranial space, a good proportion of cases tend to be located around the midline. Review of the literature as well as our own three cases--which forms the basis of this article--shows that they are mostly asymptomatic.
P O, Eghwrudjakpor +3 more
openaire +2 more sources
Archives of Surgery, 1983
We reviewed 15 years of experience with gastrointestinal (GI) lipomas at our institution. A series of eight patients was included, six of whom had lipomas in the colon and two, in the stomach. All eight patients were symptomatic. The diagnosis was not made preoperatively in seven cases, which accounted for surgical intervention in these patients ...
M J, Fernandez, R P, Davis, P F, Nora
openaire +2 more sources
We reviewed 15 years of experience with gastrointestinal (GI) lipomas at our institution. A series of eight patients was included, six of whom had lipomas in the colon and two, in the stomach. All eight patients were symptomatic. The diagnosis was not made preoperatively in seven cases, which accounted for surgical intervention in these patients ...
M J, Fernandez, R P, Davis, P F, Nora
openaire +2 more sources
Clinical Orthopaedics and Related Research, 1983
Intraosseous lipoma is the rarest benign primary tumor of bone. The incidence is less than one per 1,000 bone tumors. Because of its rarity and non-specific clinicopathologic findings, large biopsy specimens are needed for an accurate diagnosis. Once diagnosis has been established, a conservative treatment protocol is mandatory.
M C, Leeson, D, Kay, B S, Smith
openaire +2 more sources
Intraosseous lipoma is the rarest benign primary tumor of bone. The incidence is less than one per 1,000 bone tumors. Because of its rarity and non-specific clinicopathologic findings, large biopsy specimens are needed for an accurate diagnosis. Once diagnosis has been established, a conservative treatment protocol is mandatory.
M C, Leeson, D, Kay, B S, Smith
openaire +2 more sources
The Journal of Laryngology & Otology, 1999
AbstractLipomas of the parapharyngeal space provide both a diagnostic and therapeutic challenge. They are extremely rare with only a few cases having been reported. We present the case of a right parapharyngeal space lipoma in a 69-year-old man that was excised via a transcervical approach.
R F, Scott, M M, Collins, J A, Wilson
openaire +2 more sources
AbstractLipomas of the parapharyngeal space provide both a diagnostic and therapeutic challenge. They are extremely rare with only a few cases having been reported. We present the case of a right parapharyngeal space lipoma in a 69-year-old man that was excised via a transcervical approach.
R F, Scott, M M, Collins, J A, Wilson
openaire +2 more sources
Acta Pathologica Microbiologica Scandinavica Series A :Pathology, 1982
In a previous clinico‐pathologic and prognostic study of a Swedish national series of liposarcoma the designation atypical lipoma was suggested for a group of well‐differentiated non‐metastasizing liposarcomas characterized by only moderate nuclear atypia. In the present report. 21 new cases of atypical lipoma are described.
Kindblom LG +2 more
openaire +3 more sources
In a previous clinico‐pathologic and prognostic study of a Swedish national series of liposarcoma the designation atypical lipoma was suggested for a group of well‐differentiated non‐metastasizing liposarcomas characterized by only moderate nuclear atypia. In the present report. 21 new cases of atypical lipoma are described.
Kindblom LG +2 more
openaire +3 more sources