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| LMDDx = [[schwannoma]], [[leiomyoma]], [[leiomyosarcoma]], [[neurofibroma]], [[desmoid-type fibromatosis]] | | LMDDx = [[schwannoma]], [[leiomyoma]], [[leiomyosarcoma]], [[neurofibroma]], [[desmoid-type fibromatosis]] | ||
| Stains = | | Stains = | ||
| IHC = CD117 +ve, | | IHC = CD117 +ve, [[DOG1]] +ve, CD34 +ve, S-100 -ve | ||
| EM = | | EM = | ||
| Molecular = mutation in KIT gene ''or'' PDGFRA gene | | Molecular = mutation in KIT gene ''or'' PDGFRA gene | ||
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| Gross = | | Gross = | ||
| Grossing = | | Grossing = | ||
| Staging = [[gastrointestinal stromal tumour staging]] | |||
| Site = [[stomach]], [[small intestine]], other sites | | Site = [[stomach]], [[small intestine]], other sites | ||
| Assdx = | | Assdx = | ||
| Syndromes = [[Neurofibromatosis type 1]], [[Carney triad]], Carney-Stratakis syndrome | | Syndromes = [[Neurofibromatosis type 1]], [[Carney triad]], [[Carney-Stratakis syndrome]] | ||
| Clinicalhx = | | Clinicalhx = | ||
| Signs = | | Signs = | ||
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===Definition=== | ===Definition=== | ||
*Tumour resulting from a mutation in the KIT gene ''or'' PDGFRA (Platelet-derived growth factor receptor, alpha polypeptide) gene.<ref name=pmid17090188/> | *Tumour resulting from a mutation in the KIT gene ''or'' PDGFRA (Platelet-derived growth factor receptor, alpha polypeptide) gene.<ref name=pmid17090188/> | ||
*Cases wild-type for KIT or PDFGRA may harbour defects in the [[succinate dehydrogenase]] complex, NF-1, BRAF, or extremely rarely KRAS. | |||
===Epidemiology=== | ===Epidemiology=== | ||
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*[[Neurofibromatosis|Neurofibromatosis 1]] (von Recklinghausen's disease). | *[[Neurofibromatosis|Neurofibromatosis 1]] (von Recklinghausen's disease). | ||
*[[Carney triad]]. | *[[Carney triad]]. | ||
*Carney-Stratakis syndrome - GISTs and [[paraganglioma]] - due to mutation in the genes for succinate dehydrogenase.<ref>{{Cite journal | last1 = Blay | first1 = JY. | last2 = Blomqvist | first2 = C. | last3 = Bonvalot | first3 = S. | last4 = Boukovinas | first4 = I. | last5 = Casali | first5 = PG. | last6 = De Alava | first6 = E. | last7 = Dei Tos | first7 = AP. | last8 = Dirksen | first8 = U. | last9 = Duffaud | first9 = F. | title = Gastrointestinal stromal tumors: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. | journal = Ann Oncol | volume = 23 Suppl 7 | issue = | pages = vii49-55 | month = Oct | year = 2012 | doi = 10.1093/annonc/mds252 | PMID = 22997454 | url = http://annonc.oxfordjournals.org/content/23/suppl_7/vii49.full }}</ref> | *[[Carney-Stratakis syndrome]] - GISTs and [[paraganglioma]] - due to mutation in the genes for [[succinate dehydrogenase]].<ref name=pmid22997454>{{Cite journal | last1 = Blay | first1 = JY. | last2 = Blomqvist | first2 = C. | last3 = Bonvalot | first3 = S. | last4 = Boukovinas | first4 = I. | last5 = Casali | first5 = PG. | last6 = De Alava | first6 = E. | last7 = Dei Tos | first7 = AP. | last8 = Dirksen | first8 = U. | last9 = Duffaud | first9 = F. | title = Gastrointestinal stromal tumors: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. | journal = Ann Oncol | volume = 23 Suppl 7 | issue = | pages = vii49-55 | month = Oct | year = 2012 | doi = 10.1093/annonc/mds252 | PMID = 22997454 | url = http://annonc.oxfordjournals.org/content/23/suppl_7/vii49.full }}</ref> | ||
===Treatment=== | ===Treatment=== | ||
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*Large size. | *Large size. | ||
**Often benign if small size. | **Often benign if small size. | ||
*High mitotic rate (for area 5mm | *High mitotic rate (for area 5mm<sup>2</sup>). | ||
*Site - small intestine GISTs worse than stomach GISTs. | *Site - small intestine GISTs worse than stomach GISTs. | ||
Small intestine bad prognosis:<ref name=pmid17090188/> | Small intestine bad prognosis:<ref name=pmid17090188/> | ||
* >5 mitoses/5 mm | * >5 mitoses/5 mm<sup>2</sup> ''or'' size >10 cm. | ||
Stomach bad prognosis:<ref name=pmid17090188/> | Stomach bad prognosis:<ref name=pmid17090188/> | ||
* >5 mitoses/5 mm | * >5 mitoses/5 mm<sup>2</sup> ''and'' size >5 cm. | ||
===Location=== | ===Location=== | ||
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Notes: | Notes: | ||
*Small intestinal GISTs have a worse prognosis than gastric ones.<ref name=pmid17090188/> | *Small intestinal GISTs have a worse prognosis than gastric ones.<ref name=pmid17090188/> | ||
*GISTs almost never metastasize to the [[lymph node]]s | *GISTs almost never metastasize to the [[lymph node]]s (except for SDH-B deficient epithelioid GISTs) | ||
**Most common [[metastasis]] locations: [[liver]], abdominal soft tissue. | **Most common [[metastasis]] locations: [[liver]], abdominal soft tissue. | ||
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** May be epithelioid (round) ~40% of tumours. | ** May be epithelioid (round) ~40% of tumours. | ||
** Mixed epithelioid and spindle cell tumours ~10% tumours. | ** Mixed epithelioid and spindle cell tumours ~10% tumours. | ||
*+/-Cytoplasmic inclusions | *+/-Cytoplasmic inclusions<ref name=pmid7757951>{{cite journal |author=Pasquinelli G, Severi B, Martinelli GN, Santini D, Gelli MC, Tison V |title=Gastro-intestinal stromal tumors: an ultrastructural reinterpretation of the clear cell component |journal=J. Submicrosc. Cytol. Pathol. |volume=27 |issue=2 |pages=251–7 |year=1995 |month=April |pmid=7757951 |doi= |url=}}</ref> - perinuclear.<ref>{{Cite journal | last1 = Boşoteanu | first1 = M. | last2 = Boşoteanu | first2 = C. | last3 = Deacu | first3 = M. | last4 = Aşchie | first4 = M. | title = Differential diagnosis of a gastric stromal tumor: case report and literature review. | journal = Rom J Morphol Embryol | volume = 52 | issue = 4 | pages = 1361-8 | month = | year = 2011 | doi = | PMID = 22203947 }}</ref> | ||
*Classically splits the layers of the ''muscularis propria'' - as this is where the ''interstitial cells of Cajal'' are located.<ref name=pmid16402273>{{cite journal |author=Agaimy A, Wünsch PH |title=Gastrointestinal stromal tumours: a regular origin in the muscularis propria, but an extremely diverse gross presentation. A review of 200 cases to critically re-evaluate the concept of so-called extra-gastrointestinal stromal tumours |journal=Langenbecks Arch Surg |volume=391 |issue=4 |pages=322–9 |year=2006 |month=August |pmid=16402273 |doi=10.1007/s00423-005-0005-5 |url=}}</ref> | *Classically splits the layers of the ''muscularis propria'' - as this is where the ''interstitial cells of Cajal'' are located.<ref name=pmid16402273>{{cite journal |author=Agaimy A, Wünsch PH |title=Gastrointestinal stromal tumours: a regular origin in the muscularis propria, but an extremely diverse gross presentation. A review of 200 cases to critically re-evaluate the concept of so-called extra-gastrointestinal stromal tumours |journal=Langenbecks Arch Surg |volume=391 |issue=4 |pages=322–9 |year=2006 |month=August |pmid=16402273 |doi=10.1007/s00423-005-0005-5 |url=}}</ref> | ||
*+/-Skenoid fibres - extracellular collagen bundles<ref name=pmid15798063/> ~ 2-5 x 60 micrometers - uncommon finding. | *+/-Skenoid fibres - extracellular collagen bundles<ref name=pmid15798063/> ~ 2-5 x 60 micrometers - uncommon finding. | ||
**Not seen in gastric GISTs.<ref name=pmid12692202/> | **Not seen in gastric GISTs.<ref name=pmid12692202/> | ||
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*CD117 +ve in 95%.<ref name=pmid17090188/> | *CD117 +ve in 95%.<ref name=pmid17090188/> | ||
**[[Mast cell]]s are the internal positive control. | **[[Mast cell]]s are the internal positive control. | ||
*DOG1 +ve.<ref name=pmid19011564>{{Cite journal | last1 = Liegl | first1 = B. | last2 = Hornick | first2 = JL. | last3 = Corless | first3 = CL. | last4 = Fletcher | first4 = CD. | title = Monoclonal antibody DOG1.1 shows higher sensitivity than KIT in the diagnosis of gastrointestinal stromal tumors, including unusual subtypes. | journal = Am J Surg Pathol | volume = 33 | issue = 3 | pages = 437-46 | month = Mar | year = 2009 | doi = 10.1097/PAS.0b013e318186b158 | PMID = 19011564 }}</ref> | *[[DOG1]] +ve.<ref name=pmid19011564>{{Cite journal | last1 = Liegl | first1 = B. | last2 = Hornick | first2 = JL. | last3 = Corless | first3 = CL. | last4 = Fletcher | first4 = CD. | title = Monoclonal antibody DOG1.1 shows higher sensitivity than KIT in the diagnosis of gastrointestinal stromal tumors, including unusual subtypes. | journal = Am J Surg Pathol | volume = 33 | issue = 3 | pages = 437-46 | month = Mar | year = 2009 | doi = 10.1097/PAS.0b013e318186b158 | PMID = 19011564 }}</ref> | ||
Others: | Others: | ||
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**Kit gene sequencing is being done more frequently as of late-- if a mutation is found it suggest the drug ''[[imatinib]]'' will be effective. | **Kit gene sequencing is being done more frequently as of late-- if a mutation is found it suggest the drug ''[[imatinib]]'' will be effective. | ||
**Exon 11 mutation associated with malignant behaviour.<ref name=pmid9916918>{{Cite journal | last1 = Lasota | first1 = J. | last2 = Jasinski | first2 = M. | last3 = Sarlomo-Rikala | first3 = M. | last4 = Miettinen | first4 = M. | title = Mutations in exon 11 of c-Kit occur preferentially in malignant versus benign gastrointestinal stromal tumors and do not occur in leiomyomas or leiomyosarcomas. | journal = Am J Pathol | volume = 154 | issue = 1 | pages = 53-60 | month = Jan | year = 1999 | doi = 10.1016/S0002-9440(10)65250-9 | PMID = 9916918 }}</ref> | **Exon 11 mutation associated with malignant behaviour.<ref name=pmid9916918>{{Cite journal | last1 = Lasota | first1 = J. | last2 = Jasinski | first2 = M. | last3 = Sarlomo-Rikala | first3 = M. | last4 = Miettinen | first4 = M. | title = Mutations in exon 11 of c-Kit occur preferentially in malignant versus benign gastrointestinal stromal tumors and do not occur in leiomyomas or leiomyosarcomas. | journal = Am J Pathol | volume = 154 | issue = 1 | pages = 53-60 | month = Jan | year = 1999 | doi = 10.1016/S0002-9440(10)65250-9 | PMID = 9916918 }}</ref> | ||
**Secondary mutations of c-kit lead to imatinib resistance,<ref name=pmid26779618>{{Cite journal | last1 = Wada | first1 = N. | last2 = Kurokawa | first2 = Y. | last3 = Takahashi | first3 = T. | last4 = Hamakawa | first4 = T. | last5 = Hirota | first5 = S. | last6 = Naka | first6 = T. | last7 = Miyazaki | first7 = Y. | last8 = Makino | first8 = T. | last9 = Yamasaki | first9 = M. | title = Detecting Secondary C-KIT Mutations in the Peripheral Blood of Patients with Imatinib-Resistant Gastrointestinal Stromal Tumor. | journal = Oncology | volume = 90 | issue = 2 | pages = 112-7 | month = | year = 2016 | doi = 10.1159/000442948 | PMID = 26779618 }}</ref> and resistance to other similar inhibitors. | |||
==Gastrointestinal stromal tumour staging== | |||
{{Main|Gastrointestinal stromal tumour staging}} | |||
GIST has its own staging. | |||
==Sign out== | ==Sign out== | ||
<pre> | |||
STOMACH (MASS), LESSER CURVE, WEDGE RESECTION: | |||
- GASTROINTESTINAL STROMAL TUMOUR (GIST). | |||
-- MARGINS NEGATIVE FOR GIST. | |||
COMMENT: | |||
The tumour stains as follows: | |||
POSITIVE: CD117, CD34. | |||
NEGATIVE: Desmin, S-100. | |||
</pre> | |||
<pre> | |||
SMALL BOWEL (ILEUM), RESECTION: | |||
- GASTROINTESTINAL STROMAL TUMOUR (GIST), LOW-GRADE, NO RISK OF | |||
PROGRESSIVE DISEASE. | |||
-- MARGINS NEGATIVE FOR GIST. | |||
-- PLEASE SEE TUMOUR SUMMARY. | |||
- THREE BENIGN LYMPH NODES. | |||
COMMENT: | |||
The tumour stains as follows: | |||
POSITIVE: CD117, CD34. | |||
NEGATIVE: Desmin, S-100. | |||
PROLIFERATION (Ki-67): <1%. | |||
</pre> | |||
====Incidental GIST==== | |||
<pre> | |||
Partial Stomach, Sleeve Gastrectomy: | |||
- Stomach wall with incidental GASTROINTESTINAL STROMAL TUMOUR (GIST), 2 mm in maximal dimension. | |||
-- Margin clear. | |||
- Gastric mucosa within normal limits. | |||
Comment: | |||
The tumour stains as follows: | |||
POSITIVE: DOG1, CD117, CD34. | |||
NEGATIVE: desmin, S-100. | |||
PROLIFERATION (Ki-67): <2%. | |||
</pre> | |||
===Staging=== | ===Staging=== | ||
*The stage is primarily determined by the tumour size and mitotic grade. | *The stage is primarily determined by the tumour size and mitotic grade. | ||
**In the stomach, the mitotic grade determines whether a given tumour is Stage I or Stage III.<ref>{{Cite journal | last1 = Coccolini | first1 = F. | last2 = Catena | first2 = F. | last3 = Ansaloni | first3 = L. | last4 = Pinna | first4 = AD. | title = Gastrointestinal stromal tumor and mitosis, pay attention. | journal = World J Gastroenterol | volume = 18 | issue = 6 | pages = 587-8 | month = Feb | year = 2012 | doi = 10.3748/wjg.v18.i6.587 | PMID = 22363128 }}</ref> | **In the stomach, the mitotic grade determines whether a given tumour is Stage I or Stage III.<ref>{{Cite journal | last1 = Coccolini | first1 = F. | last2 = Catena | first2 = F. | last3 = Ansaloni | first3 = L. | last4 = Pinna | first4 = AD. | title = Gastrointestinal stromal tumor and mitosis, pay attention. | journal = World J Gastroenterol | volume = 18 | issue = 6 | pages = 587-8 | month = Feb | year = 2012 | doi = 10.3748/wjg.v18.i6.587 | PMID = 22363128 }}</ref> | ||
===Micro=== | |||
The sections show a spindle cell lesion that is well-circumscribed and without significant | |||
nuclear pleomorphism. No lymphocytic cuff is surrounding the lesion. The lesion is focally | |||
seen at the inked soft tissue margin. Three mitoses are seen in 5 mm*mm. | |||
==See also== | ==See also== |
edits