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Soft Tissue Tumors

Lipoblastoma / lipoblastomatosis

 

Author: Nat Pernick, M.D., PathologyOutlines.com, Inc.

Reviewer: David Lucas, M.D., University of Michigan Health Systems (January 2009)

Revised: 26 June 2009, last major update June 2009

 

Definition

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● Lobulated tumor, either localized (lipoblastoma) or diffuse (lipoblastomatosis), resembling fetal adipose tissue

 

Terminology

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Lipoblastoma: also called fetal/embryonal lipoblastoma; well circumscribed and subcutaneous

Lipoblastomatosis: deep-seated and ill-defined

 

Epidemiology

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● Rare; infants and young children age 3 years or less (rarely ages 14-24 years), 80% are boys

 

Sites

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● Extremities, trunk, head and neck

● Occasionally mediastinum, retroperitoneum or inguinal region

 

Clinical

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● Usually presents as painless superficial soft tissue mass, 75% on left side

● If not removed, matures into lipoma but with prominent fibrous septa

● FISH is helpful to confirm diagnosis (Histopathology 2008;52:294)

 

Case reports

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● 10 month old girl with 17 cm omental tumor (J Pediatr Surg 2007;42:1149)

● 1 year old boy with cervical mass (Case of Week #123)

● 1 year old boy with scrotal tumor and complex karyotype (Archives 2004;128:797)

● Buttock lesions (J Pediatr Orthop B 2006;15:356)

 

Treatment and prognosis

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● Complete excision, but with sparing of neurovascular bundle in large tumors (J Pediatr Surg 2008;43:1295)

● 14% recur due to incomplete removal (particularly lipoblastomatosis, AJSP 1997;21:1131)

● Does not metastasize

● Follow up for 3+ years is recommended (Pediatr Surg Int 2005;21:809)

 

Gross description

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● Soft, lobulated; usually 2-5 cm, mucoid cut surface

 

Gross images

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Mucoid cut surface

 

Micro description

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● Hypocellular lobules of adipocytes in various stages of differentiation including preadipocytes (spindle or stellate shaped), uni- or multi-vacuolated lipoblasts and mature adipocytes in central lobule

● Separated by prominent fibrous septa that may be cellular

● Has plexiform vascular pattern and abundant myxoid stroma

● May have prominent extracellular mucinous pools

● Resembles fetal fat and myxoid liposarcoma

Lipoblastomatosis: less lobulation; infiltrates skeletal muscle

 

Micro images

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Lobular architecture with                Plexiform vascular pattern              Resembles lipoma with

prominent fibrous septa                   with myxoid matrix and                    minimal myxoid stroma

                                                                small fat cells

 

 

         

1 year old boy with neck mass

 

 

                               

Lobulated tumor with prominent fibrous septa                          Resembles myxoid                           

                                                                                                                liposarcoma

 

 

                       

Various images                                  Patterns

 

 

Other images: scapula tumor #1#2#3#4

 

Cytology description

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● Moderate to poorly cellular; clusters of lipocytes, lipoblasts, spindle cells

● Background of myxoid material and naked oval nuclei (Diagn Cytopathol 2005;33:195)

 

Cytology images

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1 year old boy with neck mass

 

Electron microscopy

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● Cells have investing basal lamina, pinocytotic vesicles, Golgi membranes, round/oval mitochondria, cytoplasmic glycogen and cytoplasmic lipid (AJSP 1980;4:163)

● Resembles myxoid liposarcoma and normal developing fat

 

Electron microscopy images

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Intracytoplasmic lipid

 

Molecular / cytogenetics

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● Rearrangement of 8q11 approximately q13 region in 82% (Cancer Genet Cytogenet 2008;183:60), includes PLAG1 gene (Am J Pathol 2001;159:955)

● Produces HAS2-PLAG1 and COL1A2-PLAG1 hybrid genes (Atlas of Genetics and Cytogenetics)

● Also polysomy for chromosome #8

 

Differential diagnosis

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● Infantile fibromatosis - fibrous tissue only but may entrap mature fat cells, no myxoid stroma, no plexiform vascular pattern

● Myxoid liposarcoma - rare in children, no distinct lobulation, usually more cellular with giant cells containing pleomorphic nuclei, different molecular abnormalities

● Well differentiated liposarcoma - rare in children, has mature fat but no lipoblasts, has spindle cells with large, deep-staining nuclei and marked nuclear enlargement or pleomorphism; low cellularity, MDM2 and CDK4 immunostains are sensitive and specific (AJSP 2005;29:1340)

 

Additional references

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Stanford University

 

End of Soft Tissue Tumors > Lipoblastoma / lipoblastomatosis

 

 

 

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