Template:Vessels, soft tissue
Contents
Arteries
Author:
Mikael Häggström [note 1]
Presentations
Gross processing
A minimal gross processing of arteries includes a longitudinal dissection and inspection of tunica intima.
Consecutive cross-sections allows for a detection and estimation of atherosclerotic stenosis.
Microscopic examination
- Confirm that it is actually an artery (may be a vein, and a neuron may look grossly like a small artery).
- Look for atherosclerosis and thrombosis.
- Classify atherosclerosis as mild, moderate or severe.
- If cross-sections were made, estimate the maximum percentage of occlusion for each artery.
Histopathology of pre-atherosclerotic intimal lesions: Intimal thickening (A) consists mainly of smooth muscle cells in a proteoglycan-rich matrix. Intimal xanthoma (B) displays intimal thickening with isolated foam cells (arrows).[1]
A progressive atherosclerotic lesion: Pathological intima thickening (A) has some extracellular lipid (EL) present deep in the lesion without true necrosis.[1]
Progressive lesion: A fibrous cap atheroma has a well-formed necrotic core (NC) containing lipids with an overlying thick fibrous cap (FC).[1]
Progressive lesion: Fibrocalcific plaques are heavily calcified lesions with or without a necrotic core.[1]
Histopathology of plaque components in atherosclerosis: (A) Intraplaque neovasculature (arrows); (B) intraplaque hemorrhage; (C) large areas of calcification seen as purple morula; (D) lumen thrombus (arrowhead); stained with hematoxylin and eosin (H&E); (E) macrophage infiltration; stained with CD68 antibodies.[1]

Microscopy report
- Classify any atherosclerosis as mild, moderate or severe.
- If cross-sections were made, state the maximum percentage of stenosis for each artery.
Example:
Sections of the three main coronary arteries reveal << mild / moderate / severe>> atherosclerosis, with approximately __%, __% and __% stenosis of the left anterior descending, left circumflex coronary artery and right coronary artery, respectively. |
Notes
- ↑ For a full list of contributors, see article history. Creators of images are attributed at the image description pages, seen by clicking on the images. See Patholines:Authorship for details.
Main page
References
- ↑ 1.0 1.1 1.2 1.3 1.4 Yang, Wen Jie; Fisher, Mark; Zheng, Lu; Niu, Chun Bo; Paganini-Hill, Annlia; Zhao, Hai Lu; Xu, Yun; Wong, Ka Sing; et al. (2017). "Histological Characteristics of Intracranial Atherosclerosis in a Chinese Population: A Postmortem Study ". Frontiers in Neurology 8. doi: . ISSN 1664-2295.
- ↑ Nat Pernick, M.D.. Eye - Orbit & optic nerve - Temporal arteritis. PathologyOutlines. Last author update: 1 February 2014. Last staff update: 29 December 2020
Image sources
Thrombus
Author:
Mikael Häggström [note 1]
Microscopic evaluation

Look for presence of fibroblasts or myofibroblasts, conferring a diagnosis of an organizing thrombus.
Reporting
Example:
Right profunda femoris artery clot, excision: Organizing thrombus. |
Notes
- ↑ For a full list of contributors, see article history. Creators of images are attributed at the image description pages, seen by clicking on the images. See Patholines:Authorship for details.
Main page
References
Image sources
Aneurysm
Author:
Mikael Häggström [note 1]
Gross processing
- Describe the shape (generally either fusiform or saccular).
- Measure the length and diameter
Make several cross-sections and look for any dissection in the wall.
Gross report
On this resource, the following formatting is used for comprehensiveness:
- Minimal depth
- (Moderate depth)
- ((Comprehensive))
(( A. Labeled -left upper extremity aneurysm. The specimen is received in formalin and consists of a segment of)) fusiformly dilated vessel measuring 11.5 cm in length and the diameter is 6.5 (x 6.5 cm). Upon sectioning, <<most \ (( __ %))>> of the area is occupied by tan-yellow to tan-red non-homogenous surface, consistent with an organized mural thrombus. (No visible wall dissection.) |
Notes
- ↑ For a full list of contributors, see article history. Creators of images are attributed at the image description pages, seen by clicking on the images. See Patholines:Authorship for details.
Main page
References
Image sources
Soft tissues
Tophus/gout
Author:
Mikael Häggström [note 1]
Preparation
A tophus specimen should be sent dry to the pathology department, and not be put in formalin.[note 2]
Gross processing
Preferably make a touch prep for polarized light microscopy. At least if urate crystals are not initially detected, take sections to be put in 100% alcohol and tell the histology lab to prepare it as per gout protocol.[note 2] With characteristic crystals on a touch prep, sections may possibly be submitted in formalin.[note 2]
Microscopy evaluation
On a touch prep, look for needle-shaped crystals of urate. On polarized light, these will have negative birefriengence.
Uric acid crystals in polarized light, showing negative birefringence, with yellow color when aligned parallel to the axis of the red compensator, and blue when aligned perpendicularly to it.[1]
Notes
Main page
References
- ↑ Bruce M Rothschild. Gout and Pseudogout Workup. Medscape. Updated: Jun 30, 2020
Image sources
Soft tissue tumor
Author:
Mikael Häggström [note 1]
Gross processing
If it appears fatty, gross and evaluate as a lipomatous tumor.
Generally sample one slice per centimeter.
Evaluation
In case of spindle cell tumors (having elongated nuclei), the following features may help to roughly classify the tumor:
- Pointed on both ends: True fibroblastic tumors
- Pointed on one end and blunted on the other ("bullet-shaped"): Neural/nerve sheath tumors (see section below)
- Blunted on both ends ("cigar-shaped"): Smooth muscle tumor
- Triangular: Myofibroblastic
In uncertain cases, the following immunohistochemistry markers are usually helpful:
- CD34, indicating a solitary fibrous tumor
- S100, indicating a neural or nerve sheath tumor (see section below)
- Desmin, indicating a muscular tumor (skeletal muscle or Smooth muscle tumor, latter also positive on SMA)[1]
- Beta catenin, indicating fibromatosis
At least in case of enlarged atypical nuclei, consider sarcoma as a differential diagnosis, and if unsure, have a low threshold for consulting with people with expertise in the matter, as the visual difference between benign and malignant spindle cells is relatively subtle. Relevant stains may include MDM2 and CDK4 for liposarcoma,[2] as well as desmin and SMA for Leiomyosarcoma.[1]
Main features of liposarcoma:[3]
- Spindle cells with enlarged, hyperchromatic nuclei.
- Apparently univacuolated adipocytes (may look normal).
- Lipoblasts (multivacuolated), but neither necessary nor sufficient for diagnosis.Leiomyosarcoma: Variable atypia, often with cytoplasmic vacuoles at both ends of nuclei, and frequent mitoses.[4]
Neural or nerve sheath tumors
Further information: Evaluation of suspected malignancies
Notes
- ↑ For a full list of contributors, see article history. Creators of images are attributed at the image description pages, seen by clicking on the images. See Patholines:Authorship for details.
Main page
References
- ↑ 1.0 1.1 Borislav A. Alexiev, M.D.. Soft tissue - Leiomyosarcoma-general. Pathology Outlines. Last author update: 29 September 2023
- ↑ 2.0 2.1 Susan Potterveld, D.O., M.P.H., Michael R. Clay, M.D.. Dedifferentiated liposarcoma. Pathology Outlines. Last author update: 14 June 2023
- ↑ Michael R. Clay, M.D.. Liposarcoma. PathologyOutlines. Topic Completed: 1 November 2017. Minor changes: 11 May 2021
- ↑ Vijay Shankar, M.D.. Soft tissue - Smooth muscle - Leiomyosarcoma - general. Pathology Outlines. Topic Completed: 1 November 2012. Revised: 11 September 2019
Image sources
Peripheral nerve sheath tumor
- REDIRECT Soft tissue tumor
Lipomatous tumor
Author:
Mikael Häggström [note 1]
Fixation
Generally 10% neutral buffered formalin.
See also: General notes on fixation
Comprehensiveness
On this resource, the following formatting is used for comprehensiveness:
- Minimal depth
- (Moderate depth)
- ((Comprehensive))
Gross processing
- Perform consecutive slicing of the entire specimen.
- Look for signs of liposarcoma: Mainly by firm volumes.[1] Color varies from yellow to white (and firm) depending on the proportion of adipocytic, fibrous and/or myxoid content.[2] Areas of fat necrosis are common in larger lesions. Rarely, infiltrative growth is seen.[2]
- Submit slices from any suspicious parts, or at least one representative slice from the specimen.[3] (A more comprehensive practice is to submit 1 section per centimeter, and 2 sections per cassette.[4])
Gross report
- Color
- Even absence of hemorrhage or necrosis.
Example:
Mass ((weighing 121 grams)) and measuring 10 x 6,5 x 3,5 cm. ((The surgical margin is intact.)) Cut sections show homogenous yellow color, with no hemorrhage or necrosis. ((The specimen is serially sectioned, and representative sections are submitted for microscopic examination in __ cassettes.)) |
See also: General notes on gross processing
Microscopic evaluation
An atypical lipomatous tumor (also termed well-differentiated liposarcoma), lipoma-like subtype. At low magnification, the majority of the tumor essentially has the look of benign mature adipocytes (except for mildly increased variation in lipid droplet sizes), but high magnification of a fibrous band shows spindle cells with enlarged, hyperchromatic nuclei. Another clue for liposarcoma is a higher variability of lipid droplet sizes.
Fibrolipoma is a lipoma with focal areas of large amounts of fibrous tissue.
A sclerotic lipoma is one step further: a predominantly fibrous lesion with focal areas of fat.[5]
If unsure of degree of fibrosis: Simply report as lipoma.Angiolipoma is a lipoma with abundant capillaries, with hyaline or fibrin (pictured) thrombi.[6]
Main features of liposarcoma:[7]
- Spindle cells with enlarged, hyperchromatic nuclei.
- Apparently univacuolated adipocytes (may look normal).
- Lipoblasts, but is neither necessary nor sufficient for diagnosis.Myxoid liposarcoma: Hypercellular solid sheets of cells lying back to back, with round cells or primitive cytomorphology.[8]
A pedunculated lipomatous skin tumor may be a pedunculated lipofibroma:
Microscopy/Histopathology report
For lipomas: (Absence of signs of malignancy.)
(Chest wall, left lateral, excision:)
((Microscopic description: Tissue composed of univacuolar fat cells and delicate and inconspicuous fibrous septa.)) |
See also: General notes on reporting
Notes
- ↑ For a full list of contributors, see article history. Creators of images are attributed at the image description pages, seen by clicking on the images. See Patholines:Authorship for details.
Main page
References
- ↑ Monica Dahlgren, Janne Malina, Anna Måsbäck, Otto Ljungberg (1997-02-13). Lilla utskärningen.
- ↑ 2.0 2.1 Andreas F Mavrogenis, Panayiotis J Papagelopoulos (2013-02-01). Soft Tissues: Well-differentiated liposarcoma. Atlas of Genetics and Cytogenetics in Oncology and Haematology.
- ↑ Pathology Department at NU Hospital Group, Sweden, 2019-2020.
- ↑ . Lipoma. Gross Pathology Manual - By The University of Chicago Department of Pathology. Retrieved on 2020-08-26.
- ↑ . Lipoma Variant: Fibrolipoma. Stanford University School of Medicine. Retrieved on 2020-02-10.
- ↑ Vijay Shankar. Soft tissue - Adipose tissue tumors - Lipoma and variants - Angiolipoma. Pathology Outlines. Topic Completed: 1 August 2012. Minor changes: 20 March 2019
- ↑ Michael R. Clay, M.D.. Liposarcoma. PathologyOutlines. Topic Completed: 1 November 2017. Minor changes: 11 May 2021
- ↑ Michael R. Clay. Soft tissue - Adipose tissue - Myxoid liposarcoma. PathologyOutlines. Topic Completed: 1 January 2018. Revised: 20 March 2019
Image sources
Hernia sac
Author:
Mikael Häggström [note 1]
Comprehensiveness
On this resource, the following formatting is used for comprehensiveness:
- Minimal depth
- (Moderate depth)
- ((Comprehensive))
Fixation
Generally 10% neutral buffered formalin.
Gross processing
A gross inspection is almost always enough, and tissue generally does not need to be submitted except in unique circumstances.[1] ((Still you may submit 1 cassette of one or more representative sections for an inguinal hernia sac in a patient aged up to 16 years of age, or in case of hernia sacs from other regions than inguinal.))
- Gross report
((A. Labeled - ___. The specimen is received in formalin and consists of)) __ fragment(s) of pink-tan fibromembranous tissue, measuring ___ cm in greatest dimension and ___ cm in greatest thickness. The surfaces are smooth. There are no sections submitted for microscopic examination. (Representative sections are submitted for microscopic examination in __ cassettes.) |
Microscopic report
In case of a gross only examination, the microscopic report may still be given as a formality:
Right inguinal region, herniorrhaphy: Hernia sac, gross examination only. |
When microscopy slides of the case are available, you may screen the sample at low magnification to rule out obvious pathology:
Umbilical hernia sac, hernia repair: Connective tissue lined by mesothelium, consistent with hernia sac. |
Notes
- ↑ For a full list of contributors, see article history. Creators of images are attributed at the image description pages, seen by clicking on the images. See Patholines:Authorship for details.
Main page
References
- ↑ Chesley PM, Black GE, Martin MJ, Johnson EK, Maykel JA, Steele SR (2015). "The utility of pathologic evaluation of adult hernia specimens. ". Am J Surg 209 (5): 783-6; discussion 786. doi: . PMID 25725504. Archived from the original. .
Image sources