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==Pathology simplified== | ==Pathology simplified== | ||
===Blue & pink=== | |||
H&E is the standard... | H&E is the standard... | ||
*Too much '''PINK''' = DEAD ([[necrosis]]). | *Too much '''PINK''' = DEAD ([[necrosis]]). | ||
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In words: | In words: | ||
*''Blue is bad and pink is dead!''<ref> | *''Blue is bad and pink is dead!''<ref>Streutker, C. 8 June 2013.</ref> | ||
Note: | Note: | ||
*Lymph | *There is a lengthy list of things that are blue and ''not'' "bad"... that why a pathology residency is years. | ||
**[[Lymph node]]s are very blue... they aren't necessarily bad. | |||
**Reactive processes can be very blue... they aren't bad. | |||
===Three questions=== | |||
Pathology can be boiled down to: | |||
#What is it? | |||
#*Biopsies. | |||
#Did I get it all? | |||
#*Resections. | |||
#Did I get the right thing? | |||
#*Most other things. | |||
==Terms== | ==Terms== | ||
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*''Argyrophilic'' means has an affinity for silver<ref>URL: [http://www.merriam-webster.com/medical/argyrophilic http://www.merriam-webster.com/medical/argyrophilic]. Accessed on: 29 August 2011.</ref><ref>URL: [http://en.wiktionary.org/wiki/argyrophilic http://en.wiktionary.org/wiki/argyrophilic]. Accessed on: 29 August 2011.</ref>/loves silver/stains with silver. | *''Argyrophilic'' means has an affinity for silver<ref>URL: [http://www.merriam-webster.com/medical/argyrophilic http://www.merriam-webster.com/medical/argyrophilic]. Accessed on: 29 August 2011.</ref><ref>URL: [http://en.wiktionary.org/wiki/argyrophilic http://en.wiktionary.org/wiki/argyrophilic]. Accessed on: 29 August 2011.</ref>/loves silver/stains with silver. | ||
===Morphologic patterns=== | ===Morphologic patterns=== | ||
{| | {{Main|Morphologic patterns}} | ||
This covers things like ''cribriform'', ''hobnail'', ''herring bone'' and many others. | |||
===Nuclear destruction words=== | ===Nuclear destruction words=== | ||
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Image: | Image: | ||
*[http:// | *[http://en.wikipedia.org/wiki/File:Nuclear_changes.jpg Karyolysis, pyknosis, karyorrhexis (WP)]. | ||
== | ===Erosions and ulcers=== | ||
*Ulcer = lesion through skin or mucous membrane. | |||
*Erosion = limited to the mucosa - superficial ulceration. | |||
**In dermatopathology - through the epidermis. | |||
Image: | |||
<gallery> | |||
Image:Ulcers,_fissures,_and_erosions.svg | Ulcers and erosions - schematic. (WC) | |||
</gallery> | |||
====Microscopic - erosion==== | |||
Features - require 1 and 2: | |||
#Loss of epithelium. | |||
#Vital response at site of lost epithelium. | |||
#*[[Neutrophil]]ic infiltrate. | |||
#*+/-Fibrin. | |||
#*+/-Cellular debris. | |||
Image: | |||
*[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400158/figure/f4-cln_67p705/ Mucosal erosion (nih.gov)].<ref name=pmid22892912>{{Cite journal | last1 = Arashiro | first1 = RT. | last2 = Teixeira | first2 = MG. | last3 = Rawet | first3 = V. | last4 = Quintanilha | first4 = AG. | last5 = Paula | first5 = HM. | last6 = Silva | first6 = AZ. | last7 = Nahas | first7 = SC. | last8 = Cecconello | first8 = I. | title = Histopathological evaluation and risk factors related to the development of pouchitis in patients with ileal pouches for ulcerative colitis. | journal = Clinics (Sao Paulo) | volume = 67 | issue = 7 | pages = 705-10 | month = Jul | year = 2012 | doi = | PMID = 22892912 | PMC = 3400158 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400158/}}</ref> | |||
==The general differential diagnosis== | |||
Mnemonic ''CINE-TV-DATE'': | Mnemonic ''CINE-TV-DATE'': | ||
*Congenital. | *Congenital. | ||
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In diagnostic pathology, most stuff falls into the ''neoplastic'' category. | In diagnostic pathology, most stuff falls into the ''neoplastic'' category. | ||
===Cytologic features | ===Features of malignancy=== | ||
It is said that | ====Cytologic features of malignancy==== | ||
It is said that:<ref name=boerner>S. Boerner. 12 September 2011.</ref> | |||
#It is the nuclear abnormalities that make a cell malignant. | #It is the nuclear abnormalities that make a cell malignant. | ||
#The cytoplasm that gives one clues as to the cell of origin. | #The cytoplasm that gives one clues as to the cell of origin. | ||
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| weak | | weak | ||
|- | |- | ||
| Nuclear-to-cytoplasmic ratio | | [[Nuclear-to-cytoplasmic ratio]] | ||
| strong | | strong | ||
|- | |- | ||
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§ mitoses are seen in poorly differentiated tumour and regeneration. High mitotic rate in the context of unremarkable nuclear morphology is usually not malignant. | § mitoses are seen in poorly differentiated tumour and regeneration. High mitotic rate in the context of unremarkable nuclear morphology is usually not malignant. | ||
=== | ====Other features==== | ||
In the context of [[soft tissue lesions]], it is said that the two most important features of malignancy are: | |||
#[[Necrosis]]. | |||
#High vascularity. | |||
Notes: | |||
*Benign soft tissue lesions may have marked [[nuclear atypia]] and abundant mitotic activity. | |||
===General differential diagnosis of malignant lesion=== | |||
This should ''always'' be considered: | This should ''always'' be considered: | ||
<center> | <center> | ||
Line 172: | Line 144: | ||
{{familytree | | | |A11| | | | |A11 = Malignancy }} | {{familytree | | | |A11| | | | |A11 = Malignancy }} | ||
{{familytree | |,|-|-|^|-|-|.|}} | {{familytree | |,|-|-|^|-|-|.|}} | ||
{{familytree | B11 | | | | B12 |B11=Primary|B12=Metastatic }} | {{familytree | B11 | | | | B12 |B11=Primary|B12=[[metastasis|Metastatic]] }} | ||
{{familytree/end}} | {{familytree/end}} | ||
</center> | </center> | ||
Q. Why? <br> | Q. Why? <br> | ||
A. (1) The site of the tumour can considerably change the differential diagnosis. (2) The management is usually totally different.<br><br> | A. (1) The site of the tumour can considerably change the differential diagnosis. (2) The management is usually totally different.<br><br> | ||
A | |||
===A general clinico-histomorphologically motivated differential diagnosis of malignancy=== | |||
<center> | <center> | ||
<!-- | <!-- | ||
Line 185: | Line 158: | ||
{{familytree | | | | | | | | | | | A | | | | | | | | | | |A=Malignancy}} | {{familytree | | | | | | | | | | | A | | | | | | | | | | |A=Malignancy}} | ||
{{familytree | |,|-|-|-|v|-|-|-|v|-|^|-|v|-|-|-|v|-|-|-|.| |}} | {{familytree | |,|-|-|-|v|-|-|-|v|-|^|-|v|-|-|-|v|-|-|-|.| |}} | ||
{{familytree | B | | C | | D | | E | | F | |G |B=Epithelial<br>(Carcinoma)|C=Mesenchymal<br>(Sarcoma)|D=[[Germ cell tumours|Germ cell<br>tumour]]|E=[[Neuroendocrine carcinoma|Neuroendocrine<br>carcinoma]]|F=Hematologic|G=[[Melanoma|Malignant<br>melanoma]]}} | {{familytree | B | | C | | D | | E | | F | |G |B=Epithelial<br>(Carcinoma)|C=Mesenchymal<br>([[Sarcoma]])|D=[[Germ cell tumours|Germ cell<br>tumour]]|E=[[Neuroendocrine carcinoma|Neuroendocrine<br>carcinoma]]|F=Hematologic|G=[[Melanoma|Malignant<br>melanoma]]}} | ||
{{familytree/end}} | {{familytree/end}} | ||
</center> | </center> | ||
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*''[[Malignant melanoma]]'', also ''melanoma'', is a separate category as it can look like almost anything under the microscope. | *''[[Malignant melanoma]]'', also ''melanoma'', is a separate category as it can look like almost anything under the microscope. | ||
*''Hematologic'' includes [[lymphoma]], [[leukemia]], [[plasma cell neoplasms]] and others. | *''Hematologic'' includes [[lymphoma]], [[leukemia]], [[plasma cell neoplasms]] and others. | ||
*The above is a useful clinical classification. The problem is it isn't that useful for difficult cases as: | |||
**Germ cell tumours are often not distinctive. | |||
**Numerous epithelioid sarcomas can mimic carcinomas. | |||
**Spindle cell carcinomas can mimic sarcomas very well. | |||
**Neuroendocrine differentiation is not always readily apparent. | |||
**The ''[[modified general morphologic DDx of malignancy]]'' is better for approaching difficult tumours. | |||
Memory device ''HMN GEM'': hematologic, melanoma, neuroendocrine carcinoma, germ cell, epithelial, mesenchymal. | |||
===Morphologic | ====Morphologic categorization==== | ||
=====Factors to consider===== | |||
Factors to consider when attempting to group by morphology: | Factors to consider when attempting to group by morphology: | ||
#Cell shape (spindle cell, epithelioid, plasmacytoid, mixed). | |||
#Cell size (small or large) - size in relation to a neutrophil or [[red blood cell]]. | |||
#Cell cohesion - dyscohesive vs. cohesive. | #Cell cohesion - dyscohesive vs. cohesive. | ||
#*If one sees several groups of 5+ cells... probably cohesive. | #*If one sees several groups of 5+ cells... probably cohesive. | ||
#*Presence of cell cohesion strongly disfavours lymphoma. | #*Presence of cell cohesion strongly disfavours lymphoma. | ||
#Cytoplasm - abundance (scant, moderate, abundant). | #Cytoplasm - abundance (scant, moderate, abundant). | ||
#*Eosinophilic cytoplasm disfavours lymphoma. | #*Eosinophilic cytoplasm disfavours lymphoma. | ||
#*Oncocytic - possessing copious eosinophilic granular cytoplasm. | |||
#**Benign lesions composed of oncocytes - oncocytoma | |||
#**Oncocytic metaplasia (alteration of cytoplasm) can effect all or a part of a lesion. | |||
#**Oncocytic neoplasms are common in the kidneys, thyroid and salivary glands. | |||
#**Oncocytic change increases with age | |||
#**May represent senescent accumulation of mitochondria in secretory epithelial. | |||
#Chromatin - coarseness (fine, granular). | #Chromatin - coarseness (fine, granular). | ||
#Nucleoli - number (absent, present, multiple). | #Nucleoli - number (absent, present, multiple). | ||
#*Large [[nucleoli]] (nucleoli seen with the 10x objective) pretty much exclude neuroendocrine. | #*Large [[nucleoli]] (nucleoli seen with the 10x objective) pretty much exclude neuroendocrine. | ||
======Types of cells====== | |||
{| class="wikitable sortable" | |||
! Type | |||
! Morphology | |||
! Significance | |||
|- | |||
* | | [[Spindle cell]] | ||
| tapered at both ends<ref>URL: [http://www.medterms.com/script/main/art.asp?articlekey=25657 http://www.medterms.com/script/main/art.asp?articlekey=25657]. Accessed on: 18 January 2010.</ref> | |||
| suggestive of sarcoma - compatible with melanoma and some carcinomas | |||
|- | |||
| Epithelioid cell | |||
| cell shape round/oval, nucleus round/oval, looks like epithelium (cell borders touch neighbouring cells - collectively form a barrier) | |||
| suggests epithelial lesion (carcinoma) - compatible with others | |||
|- | |||
| [[Small round blue cell tumour]]/lymphoid: | |||
| small cells with scant cytoplasm - usually round; "small" is classically 2x a "resting lymphocyte" diameter † | |||
| common in children; in adults often lymphoma | |||
|- | |||
| Small lymphoid ([[small cell lymphoma]]). | |||
| "small" in the context of lymphoid is classically ~1x a "resting lymphocyte" diameter; often not malignant by cytology | |||
| suggests [[small cell lymphoma]], reactive changes or infection | |||
|- | |||
| Plasmacytoid cell | |||
| resemble a plasma cell: eccentric nucleus, moderate basophilic cytoplasm, +/-"clockface" chromatin pattern (clumping of chromatin at the periphery of the nucleus), +/-perinuclear hof (crescentic cytoplasmic clearing adjacent to the nucleus; represents abundant Golgi apparatus | |||
| suggests [[plasma cell neoplasm]] or infection | |||
|} | |||
Note: | |||
*† Diameter of a "resting lymphocyte" ~ diameter of a [[red blood cell]] (RBC) ~ 8 micrometres. | |||
**Most carcinoma cells are 3-4x the size of a RBC. | |||
====Dyscohesive | ======Dyscohesive versus cohesive====== | ||
Deciding cells are dyscohesive vs. cohesive is important, as it is a strong determinant of whether one is dealing with a lymphoid lesion or not. | Deciding cells are dyscohesive vs. cohesive is important, as it is a strong determinant of whether one is dealing with a lymphoid lesion or not. | ||
{| class="wikitable" | {| class="wikitable sortable" | ||
!| | !| | ||
!| Cell spacing | !| Cell spacing | ||
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*Basophilic cytoplasm. | *Basophilic cytoplasm. | ||
=== | =====Probable category by morphology===== | ||
*Carcinoma = cohesive, relatively large (>~2X neutrophil), +/-nucleolus, +/-gland formation (circular structures), often moderate to abundant cytoplasm. | |||
* | *Sarcoma = cohesive, composed of spindle cells (cells taper at both ends, nucleus oval/cigar-shaped). | ||
* | *Germ cell tumour = appearance often similar to ''carcinoma'', site (location) very useful - esp. gonadal, midline, retroperitoneal. | ||
* | *[[Neuroendocrine carcinoma]] = cohesive, fine granular chromatin and no [[nucleolus]]. | ||
*Lymphoma = dyscohesive, relatively small (usually <=2X neutrophil diameter), usu. scant basophilic (blue) cytoplasm. | |||
* | *Melanoma = classically pigmented, often a prominent [[red nucleolus]], a mix of spindle cells and epithelioid cells, mix of cohesive and dyscohesive cells. | ||
===A practical histomorphologic differential diagnosis of malignancy=== | |||
====General morphologic DDx of malignancy==== | |||
{{familytree/start}} | |||
{{familytree | | | | | | | A01 | | | | | | | | A01=Malignancy}} | |||
{{familytree | |,|-|-|-|v|-|^|-|v|-|-|-|.| | |}} | |||
{{familytree | B01 | | B02 | | B03 | | B04 | |B01=[[Large epithelioid tumours]]|B02=[[spindle cell lesions|Spindle cell tumours]]|B03=[[small round cell tumours|Small blue cell tumours]]|B04=[[Pleomorphic tumours]]}} | |||
{{familytree/end}} | |||
====Modified general morphologic DDx of malignancy==== | |||
<center> | |||
{{familytree/start}} | |||
{{familytree | | | | | | | | | | | A | | | | | | | | | | |A=Malignancy}} | |||
{{familytree | |,|-|-|-|v|-|-|-|v|-|^|-|v|-|-|-|v|-|-|-|.| |}} | |||
{{familytree | B | | C | | D | | E | | F | |G |B=[[Large epithelioid tumours]]|C=[[spindle cell lesions|Spindle cell tumours]]|D=[[small round cell tumours|Small blue cell tumours]]|E=[[Pleomorphic tumours]]|F=[[Clear cell tumours]]|G=[[myxoid lesions|Myxoid tumours]]}} | |||
{{familytree/end}} | |||
</center> | |||
The above is more useful than the ''general clinico-histomorphologically motivated differential diagnosis of malignancy''. | |||
==Differential diagnosis by site== | |||
{{Main|Short power list}} | |||
It is essential to have a concept of what is common. The ''[[short power list]]'' gives a short [[differential diagnosis]] for the common sites. | |||
{{Main|Long power list}} | |||
The ''[[long power list]]'' is a longer list for the common sites. | |||
==Finding the elements== | ==Finding the elements== | ||
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*Apoptotic cell -- has nuclear condensation (pyknosis), eosinophilic cytoplasm. | *Apoptotic cell -- has nuclear condensation (pyknosis), eosinophilic cytoplasm. | ||
Images: | ====Images==== | ||
<gallery> | |||
Image:Atypical_mitosis.jpg| Mitoses and an atypical mitosis. (WC) | |||
Image:Tripolar_Mitosis_-_breast_carcinoma.jpg| Tripolar mitosis. (WC) | |||
</gallery> | |||
www: | |||
*[http://education.vetmed.vt.edu/Curriculum/VM8054/Labs/Lab4/IMAGES/MITOSIS%20IN%20GUT.JPG Mitoses (vetmed.vt.edu)]. | *[http://education.vetmed.vt.edu/Curriculum/VM8054/Labs/Lab4/IMAGES/MITOSIS%20IN%20GUT.JPG Mitoses (vetmed.vt.edu)]. | ||
*[http://www.flickr.com/photos/euthman/426956752/ Starburst mitosis (flicker.com)]. | *[http://www.flickr.com/photos/euthman/426956752/ Starburst mitosis (flicker.com)]. | ||
====Phases of mitosis==== | ====Phases of mitosis==== | ||
*Prophase | *Prophase - chromatin condenses to chromosomes. | ||
*Metaphase - chromosome aligned. | *Metaphase - chromosome aligned. | ||
*Anaphase - spindles separated. | *Anaphase - spindles separated. | ||
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*A collection of PMNs... think about ''necrosis'' and ''abscess''. | *A collection of PMNs... think about ''necrosis'' and ''abscess''. | ||
===Lymph node | ===Lymph node metastasis=== | ||
{{Main|Lymph node metastasis}} | {{Main|Lymph node metastasis}} | ||
*Take a good to look at the tumour first. | *Take a good to look at the tumour first. | ||
*Tumour in a node is often better differentiated than the most poorly differentiated part in the primary site. | *Tumour in a node is often better differentiated than the most poorly differentiated part in the primary site. | ||
*Subcapsular space - the first place to look for mets. | *Subcapsular space - the first place to look for mets. | ||
*Lymph node | *Lymph node metastasis are usually obvious. | ||
*Histiocytes may be difficult to separate from tumour - especially | **There are of course exceptions, e.g. [[small cell carcinoma]], [[invasive lobular carcinoma]]. | ||
**Histiocytes | *Histiocytes may be difficult to separate from tumour - especially for the novice. | ||
**Malignant cells, generally, have to have malignant features, i.e. the NC ratio is abnormal, there is [[nuclear pleomorphism]]. | **Histiocytes may be found in the germinal centres, i.e. the node architecture helps. | ||
**Malignant cells, generally, have to have malignant features, i.e. the [[NC ratio]] is abnormal, there is [[nuclear pleomorphism]]. | |||
*Several things can mimic metastases - see ''[[Lymph node metastasis]]''. | *Several things can mimic metastases - see ''[[Lymph node metastasis]]''. | ||
See: ''[[Lymph node]]'' article for a detailed description of cell types in a lymph node. | See: ''[[Lymph node]]'' article for a detailed description of cell types in a lymph node. | ||
===Signet ring | ===Signet ring cell carcinoma=== | ||
{{Main|Signet ring cell carcinoma}} | |||
*It has been said that there are two types of pathologists... those that have missed SRCs ''and'' those that will miss SRCs. | |||
* | |||
Microscopic: | |||
* | *Cells resemble signet rings: | ||
**They contain a large amount of mucin, which pushes the nucleus to the cell periphery. | |||
**The pool of mucin in a signet ring cell mimics the appearance of a finger hole. | |||
**The nucleus mimics the appearance of the face of the ring in profile. | |||
*Cells typically 2-3x the size of a lymphocyte. | |||
**Smaller than the typical adipocyte. | **Smaller than the typical adipocyte. | ||
*Often have a | *Often have a crescent-shaped ''or'' ovoid nucleus. | ||
**Capillaries sectioned on their lumen have endothelial cells-- the nuclei of these are more spindled. | **Capillaries sectioned on their lumen have endothelial cells -- the nuclei of these are more spindled. | ||
*SRCs are usually close to friend | *SRCs are usually close to friend -- another SRC. | ||
**This helps differentiate SRCs from capillaries sectioned on their lumen. | **This helps differentiate SRCs from capillaries sectioned on their lumen. | ||
*The mucin is often clear on H&E... but maybe eosinophilic. | *The mucin is often clear on H&E... but maybe eosinophilic. | ||
DDx: | |||
*[[Fat atrophy]]. | |||
Stains: | Stains: | ||
Line 341: | Line 378: | ||
*Alican blue-PAS stain. | *Alican blue-PAS stain. | ||
Images | ====Images==== | ||
<gallery> | |||
Image:Signet_ring_cells_5.jpg |SRCs - H&E stain. (WC/Nephron) | |||
*[http:// | Image:Gastric_signet_ring_cell_carcinoma_histopatholgy_(2)_PAS_stain.jpg | SRCs - AL-PAS stain. (WC) | ||
Image:Gastric_signet_ring_cell_carcinoma_histopatholgy_(1).jpg | SRC - H&E stain. (WC) | |||
</gallery> | |||
www: | |||
*[http://www.engravingarts.com/sales/LVX2.jpg Signet rings (engravingarts.com)]. | |||
===Necrosis=== | ===Necrosis=== | ||
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*[http://www.nature.com/bmt/journal/v39/n9/fig_tab/1705646f1.html Necrosis (nature.com)]. | *[http://www.nature.com/bmt/journal/v39/n9/fig_tab/1705646f1.html Necrosis (nature.com)]. | ||
*[http://moon.ouhsc.edu/kfung/jty1/Com08/Com08Image/Com801-1-09.gif Necrosis (ouhsc.edu)].<ref>URL: [http://moon.ouhsc.edu/kfung/jty1/Com08/Com801-1-Diss.htm http://moon.ouhsc.edu/kfung/jty1/Com08/Com801-1-Diss.htm]. Accessed on: 3 November 2010.</ref> | *[http://moon.ouhsc.edu/kfung/jty1/Com08/Com08Image/Com801-1-09.gif Necrosis (ouhsc.edu)].<ref>URL: [http://moon.ouhsc.edu/kfung/jty1/Com08/Com801-1-Diss.htm http://moon.ouhsc.edu/kfung/jty1/Com08/Com801-1-Diss.htm]. Accessed on: 3 November 2010.</ref> | ||
<gallery> | |||
Image:Cat_scratch_disease_-_very_high_mag.jpg | Necrosis in [[cat scratch disease]]. (WC/Nephron) | |||
Image:Histiocytic_necrotizing_lymphadenitis_-_very_high_mag.jpg | Necrosis in [[histiocytic necrotizing lymphadenitis]]. (WC/Nephron) | |||
Image:Systemic_lupus_erythematosus_lymphadenopathy_-_high_mag.jpg | Necrosis in [[SLE lymphadenopathy]]. (WC/Nephron) | |||
</gallery> | |||
==Granulomas== | ==Granulomas== | ||
{{Main|Granuloma}} | |||
==Common morphologic problems== | ==Common morphologic problems== | ||
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*'''S'''mooth muscle cells (SMCs). | *'''S'''mooth muscle cells (SMCs). | ||
Images: | =====Images===== | ||
<gallery> | |||
Image:Cardiac_amyloidosis_high_mag_he.jpg | Cardiac amyloid. (WC/Nephron) | |||
Image:Laminations_in_a_thrombus_-_high_mag.jpg | Fibrin in a thrombus. (WC/Nephron) | |||
Image:Ovarian_fibroma_-_high_mag.jpg | Collagen in an ovarian fibroma. (WC/Nephron) | |||
Image:Glatte_Muskelzellen.jpg | Smooth muscle. (WC/Polarlys) | |||
</gallery> | |||
====Smooth muscle cells (SMCs) vs. fibrous tissue==== | ====Smooth muscle cells (SMCs) vs. fibrous tissue==== | ||
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*Schwann cells (found in nerve): nuclei = wavy appearance, thin. (???) | *Schwann cells (found in nerve): nuclei = wavy appearance, thin. (???) | ||
=== | ===Pigmented material=== | ||
*[[AKA]] brown/black granular crap. | |||
DDx of granular stuff/pigment: | DDx of granular stuff/pigment: | ||
#Lipofuscin - especially in old people. | #Lipofuscin - especially in old people. | ||
#Hemosiderin. | #Hemosiderin. | ||
#Bile - found in hepatocytes, yellow. | #Bile - found in hepatocytes, yellow. | ||
#Foreign material (tattoo pigment, anthracotic pigment). | #Foreign material (tattoo pigment, anthracotic pigment, [[amalgam tattoo]]). | ||
#Melanin. | #Melanin. | ||
Notes: | Notes: | ||
*Granular stuff should prompt consideration of ''malignant melanoma''. | *Granular stuff should prompt consideration of ''malignant melanoma''. | ||
*Memory device | *Memory device ''BH MILF'' = Bile, Homogentisic acid, Melanin, Iron (hemosiderin), Lipofuscin, Foreign material. | ||
*''Homogentisic acid'' found in ''alkaptonuria'',<ref name=Ref_PCPBoD8_20>{{Ref PCPBoD8|20}}</ref>can be considered the sixth (black) pigment. | *''Homogentisic acid'' found in ''alkaptonuria'',<ref name=Ref_PCPBoD8_20>{{Ref PCPBoD8|20}}</ref>can be considered the sixth (black) pigment. | ||
**Gentisic = jen-TIS-ik.<ref>URL: [http://dictionary.reference.com/browse/gentisic+acid http://dictionary.reference.com/browse/gentisic+acid]. Accessed on: 11 January 2012.</ref> | |||
====[[Stains]] that can help sort it out==== | ====[[Stains]] that can help sort it out==== | ||
*Prussian blue (iron stain) for hemosiderin. | *Prussian blue (iron stain) for hemosiderin. | ||
*Melan A for melanin. | *[[Fontana-Masson stain]] (or ''Melan A'') for melanin. | ||
*[[PAS stain]]<ref name=pmid5463681 >{{cite journal |author=Kovi J, Leifer C |title=Lipofuscin pigment accumulation in spontaneous mammary carcinoma of A/Jax mouse |journal=J Natl Med Assoc |volume=62 |issue=4 |pages=287–90 |year=1970 |month=July |pmid=5463681 |pmc=2611776 |doi= |url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2611776/pdf/jnma00512-0077.pdf}}</ref> ''or'' Kluver-Barrera for lipofuscin. | *[[PAS stain]]<ref name=pmid5463681 >{{cite journal |author=Kovi J, Leifer C |title=Lipofuscin pigment accumulation in spontaneous mammary carcinoma of A/Jax mouse |journal=J Natl Med Assoc |volume=62 |issue=4 |pages=287–90 |year=1970 |month=July |pmid=5463681 |pmc=2611776 |doi= |url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2611776/pdf/jnma00512-0077.pdf}}</ref> ''or'' Kluver-Barrera for lipofuscin. | ||
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{{main|Pathology and food}} | {{main|Pathology and food}} | ||
==Tumour remaining== | |||
{{Main|Surgical margins}} | |||
''R classification'':<ref>URL: [http://www.informedicalcme.com/colon-cancer/tnm-stage-groupings/ http://www.informedicalcme.com/colon-cancer/tnm-stage-groupings/]. Accessed on: 27 March 2012.</ref> | |||
*"RX resection" = residual tumour cannot be assessed. | |||
*"R0 resection" = clean margin macroscopically & microscopically. | |||
*"R1 resection" = microscopic tumour left. | |||
*"R2 resection" = macroscopic tumour left. | |||
Surgeons use this terminology. Essentially, it is the margin status. It is nice when the surgeon's assessment and the pathologist's are in agreement. | |||
=== | Note: | ||
*Generally, positive margins suck. For example, in locally advanced rectal cancer, in one study,<ref name=pmid17614249>{{cite journal |author=Larsen SG, Wiig JN, Dueland S, Giercksky KE |title=Prognostic factors after preoperative irradiation and surgery for locally advanced rectal cancer |journal=Eur J Surg Oncol |volume=34 |issue=4 |pages=410–7 |year=2008 |month=April |pmid=17614249 |doi=10.1016/j.ejso.2007.05.012 |url=}}</ref> five year survival was found to be 60%, 31% and 0% for R0, R1, and R2 resections respectively. | |||
==Clinician talk== | |||
===Performance status=== | |||
*ECOG - score from 1-5 for performance status.<ref name=pmid7165009>{{cite journal |author=Oken MM, Creech RH, Tormey DC, ''et al.'' |title=Toxicity and response criteria of the Eastern Cooperative Oncology Group |journal=Am. J. Clin. Oncol. |volume=5 |issue=6 |pages=649–55 |year=1982 |month=December |pmid=7165009 |doi= |url=}}</ref> | *ECOG - score from 1-5 for performance status.<ref name=pmid7165009>{{cite journal |author=Oken MM, Creech RH, Tormey DC, ''et al.'' |title=Toxicity and response criteria of the Eastern Cooperative Oncology Group |journal=Am. J. Clin. Oncol. |volume=5 |issue=6 |pages=649–55 |year=1982 |month=December |pmid=7165009 |doi= |url=}}</ref> | ||
**ECOG = Eastern Cooperative Oncology Group. | **ECOG = Eastern Cooperative Oncology Group. | ||
Line 590: | Line 546: | ||
Note: | Note: | ||
*Most | *Most modern [[microscope]]s, have an eye piece diameter of 22 mm. Therefore, the field diameter at 40 X is approximately 22 mm / 40 X ~= 0.55 mm and the field of view is pi/4*(0.55 mm)^2 = 0.2376 mm^2. | ||
==Pathology reports== | ==Pathology reports== | ||
{{Main|Pathology reports}} | |||
The key point in report writing is that the report should be precise, complete and easy-to-understand. | |||
===Standards=== | ===Standards=== | ||
There is no universal standard; however, there is a push to standardize by the ''Association of Directors of Anatomic and Surgical Pathology'',<ref>URL: [http://www.adasp.org/papers/position/Standardization.htm http://www.adasp.org/papers/position/Standardization.htm]</ref> among others. | |||
====Checklists==== | ====Checklists==== | ||
{{Main|CAP checklists}} | |||
The College of American Pathologists (CAP) has checklists for cancer - [http://www.cap.org/apps/cap.portal?_nfpb=true&cntvwrPtlt_actionOverride=%2Fportlets%2FcontentViewer%2Fshow&_windowLabel=cntvwrPtlt&cntvwrPtlt%7BactionForm.contentReference%7D=committees%2Fcancer%2Fcancer_protocols%2Fprotocols_index.html&_state=maximized&_pageLabel=cntvwr CAP protocols]. | The College of American Pathologists (CAP) has checklists for cancer - [http://www.cap.org/apps/cap.portal?_nfpb=true&cntvwrPtlt_actionOverride=%2Fportlets%2FcontentViewer%2Fshow&_windowLabel=cntvwrPtlt&cntvwrPtlt%7BactionForm.contentReference%7D=committees%2Fcancer%2Fcancer_protocols%2Fprotocols_index.html&_state=maximized&_pageLabel=cntvwr CAP protocols]. | ||
Line 608: | Line 562: | ||
Surgeons know that checklists work and that they save lives.<ref name=pmid19158173>{{cite journal |author=Soar J, Peyton J, Leonard M, Pullyblank AM |title=Surgical safety checklists |journal=BMJ |volume=338 |issue= |pages=b220 |year=2009 |pmid=19158173 |doi= |url=http://bmj.com/cgi/pmidlookup?view=long&pmid=19158173}}</ref> | Surgeons know that checklists work and that they save lives.<ref name=pmid19158173>{{cite journal |author=Soar J, Peyton J, Leonard M, Pullyblank AM |title=Surgical safety checklists |journal=BMJ |volume=338 |issue= |pages=b220 |year=2009 |pmid=19158173 |doi= |url=http://bmj.com/cgi/pmidlookup?view=long&pmid=19158173}}</ref> | ||
Pilots have been using checklists since the 1930s. | Pilots have been using checklists since the 1930s. | ||
===Standard diagnostic notation=== | ===Standard diagnostic notation=== | ||
Line 621: | Line 573: | ||
Gallbladder, cholecystectomy:<br> | Gallbladder, cholecystectomy:<br> | ||
- Acute cholecystitis. | - Acute cholecystitis. | ||
==Lab talk== | |||
{{Main|Cutting}} | |||
Tissue cutting terms - these often vary from lab-to-lab:<ref>URL: [http://www.mailman.srv.ualberta.ca/pipermail/patho-l/2002-July/016955.html http://www.mailman.srv.ualberta.ca/pipermail/patho-l/2002-July/016955.html]. Accessed on: 18 October 2011.</ref> | |||
*Recut = cut off the top of the block. | |||
*Serial sections = make several cuts off the top of the block and look at all of 'em. | |||
*Level = trim the block ~30 micrometres --throw away trimmed tissue-- and then cut a section to look at. | |||
*Deeper = trim the block ~100 micrometres --throw away trimmed tissue-- and then cut a section to look at. | |||
==See also== | ==See also== | ||
*[[Granulation tissue]]. | *[[Granulation tissue]]. | ||
*[[No truth in names]]. | |||
*[[Blood work]]. | |||
*[[Quality]]. | |||
==References== | ==References== |
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