1.Atypical ossifying fibromyxoid tumor: a case report and literature review.
Yuan HUANG ; Huan-Jin LOU ; Wei-Bo MAO ; Wei GONG ; Yi-Ling ZHU
Chinese Journal of Pathology 2008;37(3):206-207
Aged
;
Female
;
Fibroma
;
pathology
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Fibroma, Ossifying
;
pathology
;
Gingival Neoplasms
;
pathology
;
Humans
2.Collagenous Fibroma (Desmoplastic Fibroblastoma) .
Muharrem DAGLI ; Adil ERYILMAZ ; Aydin ACAR ; Sezer KULACOGLU ; Halit AKMANSU
Yonsei Medical Journal 2004;45(5):941-943
A Collagenous Fibroma (Desmoplastic Fibroblastoma) is a rare, benign, slowly growing, fibroblastic, soft tissue lesion. Here, the case of a 28-year-old woman, who presented with a 1-year history of a slowly growing painless mass in the right anterior aspect of her neck, is described. This type of tumor was first described by Evans in 1995, and named as a Desmoplastic fibroblastoma but was renamed, by Nielsen in 1996 as a Collagenous Fibroma. This type of tumor is frequently reported in men with a mean age at occurance of 50 years. Clinically, a Collagenous fibroma presents as a firm, well-circumscribed subcutaneous, or intramuscular, painless mass of long duration. They are mostly located in the neck and extremities. The tumors range in size from 1 to 20 cm and predominantly occurs within the subcutaneous tissue, but fascial and skeletal muscle involvement is common. The treatment of a Collagenous Fibroma is a total surgical excision. No tumor recurrence has been reported the literature during the follow-up period and no tumor recurrence was observed in our case at the 1-year follow-up.
Adult
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Female
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Fibroma, Desmoplastic/*pathology
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Humans
;
Soft Tissue Neoplasms/*pathology
3.Testicular cellular fibroma: a clinicopathological observation.
Fu-Jin LIU ; Li-Ping LIU ; Hong-Juan CHU ; Wen-Chuan WU ; Su YUAN
National Journal of Andrology 2013;19(6):535-538
OBJECTIVETo investigate the clinicopathological characteristics, differential diagnosis and prognosis of testicular cellular fibroma.
METHODSWe comprehensively analyzed the clinical presentation, histomorphology and immunohistochemistry of a case of testicular cellular fibroma, reviewed the relevant literature, and discussed its pathological features and differential diagnosis.
RESULTSA 30-year-old man presented with complaint of discomfort and painless enlargement in the right testis. The tumor was found to be a testicular fibroma characterized by a solid, thickly or thinly encapsulated, circumscribed and gray-white mass. Microscopically, fusiform cells were arranged into a storiform and herringbone pattern or fascicles. The tumor exhibited a great deal of cellularity and no nuclear polymorphisms, with a mitotic rate of 0-1/10 HP. Immunohistochemistry showed that the tumor cells were positive for Vimentin, patchily positive for S-100 and SMA, but negative for Desmin, alpha-inhibin, CD34 and CD99. The positive rate of Ki-67 was less than 1%.
CONCLUSIONTesticular cellular fibroma is a rare testicular sex cord stromal tumor, pathologically resembling its ovarian counterpart. It can be distinguished from other testicular spindle cell tumors by morphology and immunohistochemical staining. For the treatment of testicular cellular fibroma, surgical resection often has a good prognosis.
Adult ; Fibroma ; pathology ; Humans ; Immunohistochemistry ; Male ; Testicular Neoplasms ; pathology
6.Superficial Fibromatosis Mimicking Glomus Tumor of the Second Toe.
Hyang Jeong JO ; Soo Uk CHAE ; Gang Deuk KIM ; Yeung Jin KIM ; Deok Hwa CHOI ; Jae In PARK
Clinics in Orthopedic Surgery 2015;7(3):418-421
Various types of tumor can occur in the subungual space, including glomus tumors, subungual exostosis, hemangioma, epidermal cysts, and malignant tumors. While fibromatosis can occur at various sites throughout the body, it is very rarely seen in the toe. Here, we are the first to report a case of superficial fibromatosis mimicking a glomus tumor in the subungual space of the second toe. The presentation of this condition shows the possibility of encountering uncommon superficial fibromatosis in the distal phalanx of the toe, and suggests that superficial fibromatosis should be included in the differential diagnosis of a glomus tumor in the toe.
Adult
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*Fibroma
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*Glomus Tumor
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Humans
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Male
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*Osteochondroma
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*Toes/pathology/surgery
8.Aggressive Fibromatosis Arising in Temporal Muscle.
Keuk Shun SHIN ; Ki Il UHM ; Young Ho LEE ; Jae Duk LEW
Yonsei Medical Journal 1986;27(2):155-158
Fibromatosis of the temporal region is extremely rare. It has also been referred to as extra-abdominal desmoid which orininates from muscle or fascia and it is a highly recurrent tumor. This paper presents a case of temporal muscle fibromatosis and a brief review of the pertinent literature.
Female
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Fibroma/pathology*
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Human
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Masticatory Muscles*/pathology
;
Middle Age
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Muscular Diseases/pathology*
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Temporal Muscle*/pathology