Primary subcutaneous myxoid liposarcoma: a clinicopathologic review of three cases with molecular confirmation and discussion of the differential diagnosis.

Abstract:

BACKGROUND:Myxoid liposarcoma typically presents as a deep-seated mass in the lower extremity of adults. Presentation as a primary subcutaneous tumor is rare. Here we discuss clinicopathologic characteristics of three such cases and their differential diagnosis to alert dermatopathologists to this unusual clinical presentation of a potentially aggressive entity. METHODS:Cases of myxoid liposarcoma were retrieved from archives and consultation files. Inclusion required location above the subcutaneous fascia with no evidence of a metastatic origin. Clinicopathologic features were retrospectively reviewed. Fluorescence in situ hybridization for DDIT3 (CHOP) gene rearrangement was performed on all cases. RESULTS:The tumors affected young adults (two males and one female, mean 36 years, range 32-40 years). No prior history of myxoid liposarcoma or deep soft tissue mass was identified. The tumors occurred in the foot, thigh and hand. All demonstrated multilobular architecture with abundant myxoid stroma, prominent branching capillary vascular network and lipoblastic differentiation. No dermal involvement was seen. Round cell features were identified in one case and represented <5% of the tumor. All patients remain disease-free following local excision only at 6, 8 and 13 months. CONCLUSIONS:Myxoid liposarcoma can rarely present as a primary subcutaneous mass and should be considered in the differential diagnosis of cutaneous myxoid tumors in adults.

journal_name

J Cutan Pathol

authors

Buehler D,Marburger TB,Billings SD

doi

10.1111/cup.12428

subject

Has Abstract

pub_date

2014-12-01 00:00:00

pages

907-15

issue

12

eissn

0303-6987

issn

1600-0560

journal_volume

41

pub_type

杂志文章
  • Unusual second malignancies following radiation therapy: subcutaneous pleomorphic rhabdomyosarcoma and cutaneous melanoma. Two case reports.

    abstract:BACKGROUND:Among nonepithelial second neoplasms which are known to be induced by irradiation, rhabdomyosarcomas are extremely rare, and melanomas are infrequent. We report a high-grade sarcoma with rhabdomyoblastic differentiation, which appeared 30 years after megavoltage irradiation for an endometrial adenocarcinoma,...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1034/j.1600-0560.2000.027008419.x

    authors: Miracco C,Materno M,De Santi MM,Pirtoli L,Ninfo V

    更新日期:2000-09-01 00:00:00

  • Lichen aureus with clonal T cells in a child possibly induced by regular consumption of an energy drink.

    abstract::Lichen aureus is a rare disease of unknown origin that is classified under the group of pigmented purpuric dermatoses. Its most important differential diagnosis is both clinically and histologically mycosis fungoides, into which the disease can proceed in very rare cases. We describe an unusual multilocular lichen aur...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2007.00918.x

    authors: Yazdi AS,Mayser P,Sander CA

    更新日期:2008-10-01 00:00:00

  • Matrical carcinoma of the skin.

    abstract::Two elderly patients with unusual hair-follicle tumors of the face are reported. The lesions showed some histologic resemblance to pilomatrixomas but differed by the presence at the advancing edge of cytologically-atypical cells without the usual shadow cell transformation and maturation of pilomatrixomas. The term ma...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1980.tb00975.x

    authors: Weedon D,Bell J,Mayze J

    更新日期:1980-02-01 00:00:00

  • De novo intraepidermal epithelioid melanocytic dysplasia as a marker of the atypical mole phenotype -- a clinical and pathological study of 75 patients.

    abstract:BACKGROUND:We encountered a distinctive pattern of dysplastic intraepidermal melanocytic proliferation, which defies classification as a dysplastic melanocytic nevus, but in which the morphologic features fall short of a diagnosis of melanoma in situ. We designate such lesions as de novo intraepidermal epithelioid mela...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.0303-6987.2005.00314.x

    authors: Sachdeva M,Frambach GE,Crowson AN,Deng AC,Mihm MC Jr,Magro CM

    更新日期:2005-10-01 00:00:00

  • Lupus erythematosus with exclusive involvement of the acrosyringia.

    abstract::Cutaneous lesions of lupus erythematosus (LE) show a broad spectrum of clinicopathologic features. Histopathologically, besides typical patterns such as interface dermatitis, perivascular lymphocytic infiltrate and dermal mucin deposits, an involvement of the eccrine structures, especially the acrosyringium, may be ob...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2009.01295.x

    authors: Fried I,Wiesner T,Cerroni L

    更新日期:2010-01-01 00:00:00

  • Myrmecia wart inclusions as an incidental histopathologic finding.

    abstract:BACKGROUND:Latent infection by human papillomavirus (HPV) has been described for genital (mucosal) and epidermodysplasia verruciformis subtypes. Only rarely has cutaneotropic, non-oncogenic HPV been found by polymerase chain reaction studies in normal skin. METHODS:We noted myrmecia wart inclusions as an incidental hi...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2012.01968.x

    authors: Wititsuwannakul J,Ko CJ

    更新日期:2012-10-01 00:00:00

  • Syphilitic gumma arising in association with foreign material.

    abstract::Until recently the number of patients with syphilis has been diminishing. Although that trend has reversed cases of tertiary syphilis are rare and often difficult to diagnose as a substantial number of patients will have a negative rapid plasma reagin. Histologically, cutaneous lesions in late stage syphilis exist in ...

    journal_title:Journal of cutaneous pathology

    pub_type:

    doi:10.1111/cup.12770

    authors: Boyd AS

    更新日期:2016-11-01 00:00:00

  • Lipomatous apocrine mixed tumor of the skin: an unusual giant lesion occurring in the breast.

    abstract::Cutaneous mixed tumors (MTs), also known as chondroid syringomas, usually arise as small nodules in the head and neck region. We describe an unusual case of a giant MT measuring 9 cm in its greatest diameter, occurring as a slowly growing pedunculated mass on the breast of a 74-year-old woman. Although MT may rarely o...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2008.01104.x

    authors: Magro G,Floridia F,Geraci G,Marino B

    更新日期:2009-06-01 00:00:00

  • Cutaneous mastocytosis with atypical mast cells and giant cytoplasmic granules.

    abstract::A 12-year-old male presented with an 8-year history of five firm cream colored papules on the right vertex of the scalp. A biopsy showed a dense infiltrate of monomorphous mast cells involving the dermis and extending into the subcutis. A relatively well-circumscribed cluster of larger cells showed pleomorphic nuclei ...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2012.01905.x

    authors: Lachapelle J,Moroz B,Nguyen VH

    更新日期:2012-08-01 00:00:00

  • Atypical fibrous histiocytoma of the skin and subcutis in childhood and adolescence.

    abstract::The authors have observed 15 examples of a distinctive fibrohistiocytic lesion in children and adolescents which they chose to designate as "atypical fibrous histiocytoma" (AFH). Patient ages ranged from 1 to 19 years (mean 9.3 yr.). Only two cases were encountered in the first year of life, but 7 were seen in childre...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1992.tb01362.x

    authors: Marrogi AJ,Dehner LP,Coffin CM,Wick MR

    更新日期:1992-08-01 00:00:00

  • Monilethrix: an ultrastructural study.

    abstract::Characteristic moniliform hairs of monilethrix were ultrastructurally examined. By scanning electron microscope, nodes and internodes were seen alternating on the affected hair; the nodes were normal in appearance and thickness, while the internodes were thin and showed ridges and flutes. By transmission electron micr...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1984.tb00412.x

    authors: Ito M,Hashimoto K,Yorder FW

    更新日期:1984-12-01 00:00:00

  • Verruciform xanthoma in association with discoid lupus erythematosus.

    abstract::Verruciform xanthoma (VX) is an uncommon lesion occurring primarily in the oral cavity. Cutaneous lesions are much less common and they preferentially arise on anogenital skin. They are not necessarily associated with a pre-existing inflammatory process. We report a VX in association with a long-standing lesion of dis...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1992.tb01359.x

    authors: Meyers DC,Woosley JT,Reddick RL

    更新日期:1992-04-01 00:00:00

  • Alpha-1 anti-trypsin deficiency and Henoch-Schönlein purpura associated with anti-neutrophil cytoplasmic and anti-endothelial cell antibodies of immunoglobulin-A isotype.

    abstract::Alpha-1 anti-trypsin (A1AT) deficiency is an inherited enzyme deficiency that manifests with fatal lung and liver complications. In addition to pulmonary and hepatic involvement, the disease has also been linked to an increased incidence of vasculitic syndromes and autoimmune diseases, including Wegener's granulomatos...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.0303-6987.2005.00304.x

    authors: Patterson CC,Ross P Jr,Pope-Harman AL,Knight DA,Magro CM

    更新日期:2005-04-01 00:00:00

  • Histiocytic sarcoma with secondary involvement of the skin and expression of CD1a: evidence of indeterminate cell differentiation?

    abstract:BACKGROUND:Histiocytic sarcoma is an exceedingly rare malignant neoplasm composed of cells with a monocyte/macrophage phenotype. In the current nosology of histiocytic neoplasms, histiocytic sarcoma is separate from indeterminate cell histiocytosis, a generally benign disorder characterized by proliferation of a CD1a+ ...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.0303-6987.2006.00453.x

    authors: Frater JL,Kling CW,Obadiah JM,Gardner LJ,Grosso LE,Resh B,Hurley MY

    更新日期:2006-06-01 00:00:00

  • Transepithelial elimination in sarcoidosis: a frequent finding.

    abstract:BACKGROUND:Transepithelial elimination is a process by which dermal materials are expelled through an active epithelial-dermal connective tissue interaction. It has been described as a regular or sporadic occurrence in a variety of dermatologic conditions, including sarcoidosis. OBSERVATION:Our patient demonstrated a ...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/cup.12253

    authors: Ismail A,Beckum K,McKay K

    更新日期:2014-01-01 00:00:00

  • Immunohistochemistry utilization in the diagnosis of melanoma.

    abstract:BACKGROUND:The use of immunohistochemical (IHC) stains in dermatopathology is commonplace; however, little is known regarding utilization trends in melanoma diagnosis. Current Medicare local coverage determinations (LCDs) state that most pigmented lesions, including melanoma, can be diagnosed using H&E alone. METHODS:...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/cup.13648

    authors: Dinehart MS,Dinehart SM,Sukpraprut-Braaten S,High WA

    更新日期:2020-05-01 00:00:00

  • Rare, risky, recurrent: An enigmatic cutaneous polyp.

    abstract::Myxofibrosarcomas (MFSs) are sarcomas most commonly seen in older patients. These are tumors of deep soft tissue seen in subcutaneous tissue and deep fascia, with frequent muscle involvement. These sarcomas are notorious for recurrences and progression to a higher grade with notable metastatic potential. They are very...

    journal_title:Journal of cutaneous pathology

    pub_type:

    doi:10.1111/cup.13432

    authors: Singh A,Brar RK,Dey B,Nigam J,Deshpande A

    更新日期:2019-05-01 00:00:00

  • Elastic fiber pattern in scleroderma/morphea.

    abstract:BACKGROUND:Scleroderma/morphea is characterized by expansion of the dermis with thickened collagen bundles and loss of CD34(+) dermal dendrocytes. Variable elastic fiber changes have been described, but to our knowledge, no systematic study of the elastic fiber pattern correlated with CD34 expression has been reported....

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2009.01201.x

    authors: Walters R,Pulitzer M,Kamino H

    更新日期:2009-09-01 00:00:00

  • Pleiotrophin expression correlates with melanocytic tumor progression and metastatic potential.

    abstract:BACKGROUND:Gene expression profiling of melanoma and nevic tissue has demonstrated that pleiotrophin (PTN) is significantly overexpressed in human melanomas. METHODS:To further evaluate PTN expression in melanocytic lesions, protein immunohistochemistry was performed on the spectrum of melanocytic lesions. RESULTS:Me...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.0303-6987.2005.00282.x

    authors: Wu H,Barusevicius A,Babb J,Klein-Szanto A,Godwin A,Elenitsas R,Gelfand JM,Lessin S,Seykora JT

    更新日期:2005-02-01 00:00:00

  • Langerhans cell histiocytosis and multiple reticulohistiocytomas in a patient with TAR syndrome: An association not previously described.

    abstract::We describe a patient with thrombocytopenia-absent radius (TAR) syndrome, multisystemic Langerhans cell histiocytosis and multiple reticulohistiocytomas. A mutational study by massive sequencing identified the Val600Glu (V600E) BRAF mutation in the Langerhans cell histiocytosis lesions, but no molecular alterations we...

    journal_title:Journal of cutaneous pathology

    pub_type:

    doi:10.1111/cup.13483

    authors: Hipólito LN,Mendoza-Cembranos MD,Villaescusa MT,Jo-Velasco M,Requena L,Alegría-Landa V

    更新日期:2019-08-01 00:00:00

  • Dermatofibroma is a clonal proliferative disease.

    abstract::Benign fibrous histiocytoma of the skin or dermatofibroma (DF) has been regarded as a fibrohistiocytic tumor. Whether DF is a neoplastic growth or a reactive process has not been settled. Since a neoplastic process is clonal in nature, clonal analysis of DF was conducted to see if DF is a clonal disease. Fresh specime...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1034/j.1600-0560.2000.027001036.x

    authors: Chen TC,Kuo T,Chan HL

    更新日期:2000-01-01 00:00:00

  • Lymphoma- and leukemia-associated cutaneous atypical CD30+ T-cell reactions.

    abstract::Cutaneous CD30+ lymphoid infiltrates appear cytologically atypical and occasionally may be misinterpreted as recurrent disease when they occur in patients treated for other primary hematologic malignancies. We recently encountered two such cases and present our findings. One patient with B-cell lymphoma and another wi...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1034/j.1600-0560.2000.027005249.x

    authors: Su LD,Duncan LM

    更新日期:2000-05-01 00:00:00

  • Keratinocyte damage in vitiligo.

    abstract::Light and electron-microscopic studies were performed on the amelanotic and adjacent normal-appearing skin in patients with vitiligo. The amelanotic skin revealed complete loss of pigment and absence of melanocytes. In addition to severe degenerative changes of melanocytes, varying degree of damage was also seen in th...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1983.tb00328.x

    authors: Bhawan J,Bhutani LK

    更新日期:1983-06-01 00:00:00

  • Basal cell carcinoma with monster cells.

    abstract::A case of basal cell carcinoma with "monster cells" is reported. Clinically, the lesion presented as a red nodule on the forearm of a 58-year-old male. The histologic picture was striking, with large, "monstrous" nuclei scattered throughout a well defined nodule. Basal cell carcinoma with monster cells appears to repr...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1993.tb01253.x

    authors: Elston DM,Bergfeld WF,Petroff N

    更新日期:1993-02-01 00:00:00

  • Unusual expression of S-100 protein in histiocytic neoplasms.

    abstract::Twenty-nine cases of histiocytic neoplasms, some resembling juvenile xanthogranuloma (JXG) and others resembling reticulohistiocytoma (RH), were evaluated. Immunohistochemical stains were performed. In this series, seven cases were identified that expressed S-100 protein positive cells. The S-100 positive cells were p...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1600-0560.1998.tb01704.x

    authors: Tomaszewski MM,Lupton GP

    更新日期:1998-03-01 00:00:00

  • Orthokeratotic Bowen disease: a histopathologic, immunohistochemical and molecular study.

    abstract:BACKGROUND:Some examples of Bowen disease lack the characteristic broad parakeratosis making their histopathologic diagnosis particularly difficult in small and incomplete biopsies. MATERIALS AND METHODS:The archives of our dermatopathology laboratory were searched for cases of Bowen disease with >75% orthokeratosis (...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/cup.12610

    authors: Idriss MH,Misri R,Böer-Auer A

    更新日期:2016-01-01 00:00:00

  • Loss of claudin-1 expression in tumor-associated vessels correlates with acquisition of metastatic phenotype in melanocytic neoplasms.

    abstract::Claudins are a family of transmembrane proteins involved in cell-to-cell adhesion and are believed to be the main component of tight junctions. Recent studies have suggested that some metastatic solid tumors lack claudin expression. It is unknown whether claudins play a role in cutaneous melanoma. Immunohistochemical ...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.0303-6987.2005.00324.x

    authors: Cohn ML,Goncharuk VN,Diwan AH,Zhang PS,Shen SS,Prieto VG

    更新日期:2005-09-01 00:00:00

  • Sub-populations of melanocytes in pigmented basal cell carcinoma: a quantitative, ultrastructural investigation.

    abstract:BACKGROUND:Pigmentation is a characteristic clinical feature of basal cell carcinomas (BCCs) in Japanese patients. The pathogenesis of melanin pigment in pigmented BCCs is poorly understood. METHODS:We have combined the techniques of morphometric analysis and electron microscopy to assess accurately the morphologic as...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1034/j.1600-0560.2001.280104.x

    authors: Lao LM,Kumakiri M,Kiyohara T,Kuwahara H,Ueda K

    更新日期:2001-01-01 00:00:00

  • Sudoriferous acrosyringeal acantholytic disease. A subset of Grover's disease.

    abstract::Three selected cases of transient acantholytic dermatosis were studied because of their definitive correlation with sweating due to fever and/ or bed-ridden situations. Biopsy specimens were serially sectioned and acantholysis was found in the acrosyringium or traced to connect to the acrosyringium in all biopsy speci...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1996.tb01289.x

    authors: Hashimoto K,Moiin A,Chang MW,Tada J

    更新日期:1996-04-01 00:00:00

  • Skin involvement as the first manifestation of breast implant-associated anaplastic large cell lymphoma.

    abstract::Breast implant-associated anaplastic large cell lymphoma (ALCL) is a newly described clinical and pathologic entity that typically presents as seroma in the fibrous scar around the implant. Less frequently, it presents as a solid peri-implant mass, and there have been no reports to date of cutaneous lesions as the pre...

    journal_title:Journal of cutaneous pathology

    pub_type:

    doi:10.1111/cup.12697

    authors: Alcalá R,Llombart B,Lavernia J,Traves V,Guillén C,Sanmartín O

    更新日期:2016-07-01 00:00:00