Difference between revisions of "PEDS5:Volunteer Assignments and Opportunities"

From Compendium of Cancer Genome Aberrations
Jump to navigation Jump to search
VisualWikitext
[checked revision][checked revision]
 
(10 intermediate revisions by the same user not shown)
Line 6: Line 6:
  
 
To volunteer, please '''[[Mailto:CCGA@cancergenomics.org <u>Contact us</u>]]''' with your page of interest.
 
To volunteer, please '''[[Mailto:CCGA@cancergenomics.org <u>Contact us</u>]]''' with your page of interest.
 +
 +
__TOC__
 
{| class="wikitable" style="margin:auto"
 
{| class="wikitable" style="margin:auto"
 
|+<big>WHO Classification of Paediatric Tumours (5th Edition) Content</big>
 
|+<big>WHO Classification of Paediatric Tumours (5th Edition) Content</big>
Line 17: Line 19:
 
!'''Notes'''
 
!'''Notes'''
 
|-
 
|-
−
|CHAPTER 2 (HAEMATOLYMPHOID DISORDERS)
+
|
 +
==== CHAPTER 2 (HAEMATOLYMPHOID DISORDERS) ====
 
|
 
|
 
----
 
----
Line 455: Line 458:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 3 (CNS TUMOURS)
+
|
 +
==== CHAPTER 3 (CNS TUMOURS) ====
 
|
 
|
 
----
 
----
Line 981: Line 985:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 4 (PERIPHERAL NEUROBLASTIC TUMOURS)
+
|
 +
==== CHAPTER 4 (PERIPHERAL NEUROBLASTIC TUMOURS) ====
 
|
 
|
 
----
 
----
Line 1,045: Line 1,050:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 5 (EYE TUMOURS)
+
|
 +
==== CHAPTER 5 (EYE TUMOURS) ====
 
|
 
|
 
----
 
----
Line 1,186: Line 1,192:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 6 (SOFT TISSUE AND BONE TUMOURS)
+
|
 +
==== CHAPTER 6 (SOFT TISSUE AND BONE TUMOURS) ====
 
|
 
|
 
----
 
----
Line 2,273: Line 2,280:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 7 (GERM CELL TUMOURS)
+
|
 +
==== CHAPTER 7 (GERM CELL TUMOURS) ====
 
|
 
|
 
----
 
----
Line 2,447: Line 2,455:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 8 (RENAL AND MALE GENITAL TUMOURS)
+
|
 +
==== CHAPTER 8 (RENAL AND MALE GENITAL TUMOURS) ====
 
|
 
|
 
----
 
----
Line 2,643: Line 2,652:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 9 (FEMALE GENITAL TUMOURS)
+
|
 +
==== CHAPTER 9 (FEMALE GENITAL TUMOURS) ====
 
|
 
|
 
----
 
----
Line 2,795: Line 2,805:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 10 (BREAST TUMOURS)
+
|
 +
==== CHAPTER 10 (BREAST TUMOURS) ====
 
|
 
|
 
----
 
----
Line 2,848: Line 2,859:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 11 (DIGESTIVE SYSTEM TUMOUR)
+
|
 +
==== CHAPTER 11 (DIGESTIVE SYSTEM TUMOURS) ====
 
|
 
|
 
----
 
----
Line 3,022: Line 3,034:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 12 (ENDOCRINE TUMOURS)
+
|
 +
==== CHAPTER 12 (ENDOCRINE TUMOURS) ====
 
|
 
|
 
----
 
----
Line 3,163: Line 3,176:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 13 (HEAD AND NECK TUMOURS)
+
|
 +
==== CHAPTER 13 (HEAD AND NECK TUMOURS) ====
 
|
 
|
 
----
 
----
Line 3,370: Line 3,384:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 14 (THORACIC TUMOURS)
+
|
 +
==== CHAPTER 14 (THORACIC TUMOURS) ====
 
|
 
|
 
----
 
----
Line 3,434: Line 3,449:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 15 (SKIN TUMOURS)
+
|
 +
==== CHAPTER 15 (SKIN TUMOURS) ====
 
|
 
|
 
----
 
----
Line 3,564: Line 3,580:
 
|
 
|
 
|-
 
|-
−
|CHAPTER 16 (GENETIC TUMOUR SYNDROMES)
+
|
 +
==== CHAPTER 16 (GENETIC TUMOUR SYNDROMES) ====
 
|
 
|
 
----
 
----
Line 3,586: Line 3,603:
 
|[[PEDS5:Neurofibromatosis_type_1|Neurofibromatosis type 1]]
 
|[[PEDS5:Neurofibromatosis_type_1|Neurofibromatosis type 1]]
 
|Disease
 
|Disease
−
|
+
|[[GTS5:Volunteer Assignments and Opportunities|See GTS5 volunteer sheet for authorship  status]]
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
 
|-
 
|-
 
|[[PEDS5:Neurofibromatosis_type_2|Neurofibromatosis type 2]]
 
|[[PEDS5:Neurofibromatosis_type_2|Neurofibromatosis type 2]]
 
|Disease
 
|Disease
−
|
+
|[[GTS5:Volunteer Assignments and Opportunities|See GTS5 volunteer sheet for authorship  status]]
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
 
|-
 
|-
 
|[[PEDS5:Tuberous_sclerosis|Tuberous sclerosis]]
 
|[[PEDS5:Tuberous_sclerosis|Tuberous sclerosis]]
Line 3,640: Line 3,657:
 
|-
 
|-
 
|[[PEDS5:Von_Hippel-Lindau_syndrome|Von Hippel-Lindau syndrome]]
 
|[[PEDS5:Von_Hippel-Lindau_syndrome|Von Hippel-Lindau syndrome]]
 +
|Disease
 +
|[[GTS5:Volunteer Assignments and Opportunities|See GTS5 volunteer sheet for authorship  status]]
 +
|N/A
 +
|N/A
 +
|N/A
 +
|N/A
 +
|N/A
 +
|N/A
 +
|N/A
 +
|-
 +
|[[PEDS5:Hereditary_phaeochromocytoma-paraganglioma_syndromes|Hereditary phaeochromocytoma-paraganglioma syndromes]]
 
|Disease
 
|Disease
 
|
 
|
Line 3,650: Line 3,678:
 
|
 
|
 
|-
 
|-
−
|[[PEDS5:Hereditary_phaeochromocytoma-paraganglioma_syndromes|Hereditary phaeochromocytoma-paraganglioma syndromes]]
+
|[[PEDS5:WAGR_syndrome|WAGR syndrome]]
 +
|Disease
 +
|[[GTS5:Volunteer Assignments and Opportunities|See GTS5 volunteer sheet for authorship status]]
 +
|N/A
 +
|N/A
 +
|N/A
 +
|N/A
 +
|N/A
 +
|N/A
 +
|N/A
 +
|-
 +
|[[PEDS5:Beckwith-Wiedemann_and_related_overgrowth_syndromes|Beckwith-Wiedemann and related overgrowth syndromes]]
 
|Disease
 
|Disease
 
|
 
|
Line 3,661: Line 3,700:
 
|
 
|
 
|-
 
|-
−
|[[PEDS5:WAGR_syndrome|WAGR syndrome]]
+
|[[PEDS5:Familial_adenomatous_polyposis|Familial adenomatous polyposis]]
−
|Disease
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|-
 
−
|[[PEDS5:Beckwith-Wiedemann_and_related_overgrowth_syndromes|Beckwith-Wiedemann and related overgrowth syndromes]]
 
−
|Disease
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|
 
−
|-
 
−
|[[PEDS5:Familial_adenomatous_polyposis|Familial adenomatous polyposis]]
 
 
|Disease
 
|Disease
−
|
+
|[[GTS5:Volunteer Assignments and Opportunities|See GTS5 volunteer sheet for authorship  status]]
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
 
|-
 
|-
 
|[[PEDS5:Lynch_syndrome|Lynch syndrome]]
 
|[[PEDS5:Lynch_syndrome|Lynch syndrome]]
 
|Disease
 
|Disease
−
|
+
|[[GTS5:Volunteer Assignments and Opportunities|See GTS5 volunteer sheet for authorship status]]
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
 
|-
 
|-
 
|[[PEDS5:Xeroderma_pigmentosum|Xeroderma pigmentosum]]
 
|[[PEDS5:Xeroderma_pigmentosum|Xeroderma pigmentosum]]
Line 3,729: Line 3,746:
 
|[[PEDS5:Li-Fraumeni_syndrome|Li-Fraumeni syndrome]]
 
|[[PEDS5:Li-Fraumeni_syndrome|Li-Fraumeni syndrome]]
 
|Disease
 
|Disease
−
|
+
|[[GTS5:Volunteer Assignments and Opportunities|See GTS5 volunteer sheet for authorship  status]]
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
 
|-
 
|-
 
|[[PEDS5:DICER1_syndrome|DICER1 syndrome]]
 
|[[PEDS5:DICER1_syndrome|DICER1 syndrome]]
 
|Disease
 
|Disease
−
|
+
|[[GTS5:Volunteer Assignments and Opportunities|See GTS5 volunteer sheet for authorship  status]]
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
 
|-
 
|-
 
|[[PEDS5:BAP1_tumour_predisposition_syndrome|BAP1 tumour predisposition syndrome]]
 
|[[PEDS5:BAP1_tumour_predisposition_syndrome|BAP1 tumour predisposition syndrome]]
Line 3,762: Line 3,779:
 
|[[PEDS5:Constitutional_mismatch_repair_deficiency_syndrome|Constitutional mismatch repair deficiency syndrome]]
 
|[[PEDS5:Constitutional_mismatch_repair_deficiency_syndrome|Constitutional mismatch repair deficiency syndrome]]
 
|Disease
 
|Disease
−
|
+
|[[GTS5:Volunteer Assignments and Opportunities|See GTS5 volunteer sheet for authorship  status]]
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
−
|
+
|N/A
 
|-
 
|-
 
|[[PEDS5:Rhabdoid_tumour_predisposition_syndrome|Rhabdoid tumour predisposition syndrome]]
 
|[[PEDS5:Rhabdoid_tumour_predisposition_syndrome|Rhabdoid tumour predisposition syndrome]]

Latest revision as of 14:11, 10 September 2024

Welcome!

For assignments, please see the "Author" column below (highlighted blue).

If empty (no name is present), please volunteer to create content for that disease!

To volunteer, please [Contact us] with your page of interest.

WHO Classification of Paediatric Tumours (5th Edition) Content
Disease Page Type Author Date Assigned to Author Target Completion Date Author Content (Pending or Complete) Date Completed by Author Associate Editor Date of Last Editor Review Notes

CHAPTER 2 (HAEMATOLYMPHOID DISORDERS)
Chronic myeloid leukaemia (CML) Disease
Juvenile myelomonocytic leukaemia Disease
Refractory cytopenia of childhood Disease
Myelodysplastic syndrome with excess blasts Disease
Acute myeloid leukaemias (AMLs) defined by differentiation Disease
Acute myeloid leukaemias (AMLs) with defining genetic abnormalities Disease
Myeloid neoplasms associated with germline predisposition Disease
Myeloid proliferations associated with Down syndrome Disease
Mastocytosis Disease
B-lymphoblastic leukaemia/lymphoma Disease
T- and NK-lymphoblastic leukaemia/lymphoma Disease
Primary mediastinal large B-cell lymphoma Disease
Diffuse large B-cell lymphoma NOS Disease
EBV-positive diffuse large B-cell lymphoma Disease
Large B-cell lymphoma with IRF4 rearrangement Disease
Paediatric-type follicular lymphoma Disease
Paediatric nodal marginal zone lymphoma Disease
ALK-positive large B-cell lymphoma Disease
Lymphomatoid granulomatosis Disease
Plasmablastic lymphoma Disease
Mediastinal grey zone lymphoma Disease
Burkitt lymphoma Disease
Large B-cell lymphoma with 11q aberration Disease
Peripheral T-cell lymphoma NOS Disease
Aggressive NK-cell leukaemia Disease
Mycosis fungoides Disease
Primary cutaneous CD30-positive T-cell lymphoproliferative disorders Disease
Subcutaneous panniculitis-like T-cell lymphoma Disease
ALK-positive anaplastic large cell lymphoma Disease
Hepatosplenic T-cell lymphoma Disease
Systemic EBV-positive T-cell lymphoma of childhood Disease
Hydroa vacciniforme lymphoproliferative disorder Disease
Classic Hodgkin lymphoma Disease
Nodular lymphocyte-predominant Hodgkin lymphoma Disease
Langerhans cell histiocytosis and related disorders Disease
Primary immunodeficiency-associated lymphoproliferative disorders Disease
Posttransplant lymphoproliferative disorders Disease
HIV-associated lymphoproliferative disorders Disease

CHAPTER 3 (CNS TUMOURS)
Diffuse astrocytoma, MYB- or MYBL1-altered Disease
Angiocentric glioma Disease
Polymorphous low-grade neuroepithelial tumour of the young Disease
Diffuse low-grade glioma, MAPK pathway-altered Disease
Diffuse midline glioma, H3 K27-altered Disease
Diffuse hemispheric glioma, H3 G34-mutant Disease
Diffuse paediatric-type high-grade glioma, H3-wildtype and IDH-wildtype Disease
Infant-type hemispheric glioma Disease
Pilocytic astrocytoma Disease
High-grade astrocytoma with piloid features Disease
Pleomorphic xanthoastrocytoma Disease
Subependymal giant cell astrocytoma Disease
Astroblastoma, MN1-altered Disease
Ganglioglioma Disease
Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma Disease
Dysembryoplastic neuroepithelial tumour Disease
Diffuse glioneuronal tumour with oligodendroglioma-like features and nuclear clusters Disease
Diffuse leptomeningeal glioneuronal tumour Disease
Multinodular and vacuolating neuronal tumour Disease
Supratentorial ependymoma Disease
Supratentorial ependymoma, ZFTA fusion-positive Disease
Supratentorial ependymoma, YAP1 fusion-positive Disease
Posterior fossa ependymoma Disease
Posterior fossa group A (PFA) ependymoma Disease
Posterior fossa group B (PFB) ependymoma Disease
Spinal ependymoma, MYCN-amplified Disease
Myxopapillary ependymoma Disease
Choroid plexus papilloma Disease
Atypical choroid plexus papilloma Disease
Choroid plexus carcinoma Disease
Medulloblastoma, WNT-activated Disease
Medulloblastoma, SHH-activated and TP53-wildtype Disease
Medulloblastoma, SHH-activated and TP53-mutant Disease
Medulloblastoma, non-WNT/non-SHH Disease
Medulloblastoma, histologically defined Disease
Atypical teratoid/rhabdoid tumour Disease
Cribriform neuroepithelial tumour Disease
Embryonal tumour with multilayered rosettes Disease
CNS neuroblastoma, FOXR2-activated Disease
CNS tumour with BCOR internal tandem duplication Disease
CNS embryonal tumour NEC/NOS Disease
Pineoblastoma Disease
Diffuse meningeal melanocytic neoplasms: Melanocytosis and melanomatosis Disease
Pituitary adenoma / pituitary neuroendocrine tumour Disease
Pituitary blastoma Disease
Adamantinomatous craniopharyngioma Disease

CHAPTER 4 (PERIPHERAL NEUROBLASTIC TUMOURS)
Ganglioneuroma Disease
Ganglioneuroblastoma, intermixed Disease
Neuroblastoma Disease
Ganglioneuroblastoma, nodular (and other composite neuroblastic tumours) Disease

CHAPTER 5 (EYE TUMOURS)
Epibulbar choristoma Disease
Epibulbar osseous choristoma Disease
Phakomatous choristoma Disease
Conjunctival junctional, compound, and subepithelial naevi Disease
Inflamed juvenile conjunctival naevus Disease
Diffuse choroidal neurofibroma and ganglioneuroma Disease
Lisch nodule (iris hamartoma) Disease
Retinocytoma Disease
Retinoblastoma Disease
Medulloepithelioma Disease
Pilocytic astrocytoma and other gliomas of the optic nerve Disease

CHAPTER 6 (SOFT TISSUE AND BONE TUMOURS)
Lipomatosis Disease
Lipoblastoma/lipoblastomatosis Disease
Liposarcoma Disease
Fasciitis/myositis Disease
Fibrodysplasia ossificans progressiva Disease
Fibroma of tendon sheath Disease
Gardner fibroma Disease
Fibrous hamartoma of infancy Disease
Lipofibromatosis Disease
Inclusion body infantile digital fibromatosis Disease
Juvenile hyaline fibromatosis (hyaline fibromatosis syndrome) Disease
Fibromatosis colli Disease
Calcifying aponeurotic fibroma Disease
Sinonasal angiofibroma Disease
Plantar/palmar fibromatoses Disease
Dermatofibrosarcoma protuberans Disease
Desmoid fibromatosis Disease
EWSR1::SMAD3-positive fibroblastic tumour Disease
Infantile fibrosarcoma Disease
Paediatric NTRK-rearranged spindle cell neoplasm Disease
Low-grade fibromyxoid sarcoma / sclerosing epithelioid fibrosarcoma Disease
Inflammatory myofibroblastic tumour Disease
Low-grade myofibroblastic sarcoma Disease
Fibrous histiocytoma Disease
Plexiform fibrohistiocytic tumour Disease
Tenosynovial giant cell tumour Disease
Capillary malformations Disease
Venous malformations Disease
Arteriovenous malformations Disease
Intramuscular vascular anomalies Disease
Lymphatic anomalies Disease
Congenital haemangioma Disease
Infantile haemangioma Disease
Haemangioma of placenta Disease
Lobular capillary haemangioma (pyogenic granuloma) Disease
Epithelioid haemangioma Disease
Tufted angioma and kaposiform haemangioendothelioma Disease
Papillary intralymphatic angioendothelioma and retiform haemangioendothelioma Disease
Pseudomyogenic haemangioendothelioma Disease
Kaposi sarcoma Disease
Epithelioid haemangioendothelioma Disease
Angiosarcoma Disease
Myofibroma and myopericytoma Disease
Glomus tumour and glomuvenous malformation Disease
EBV-associated smooth muscle tumour Disease
Rhabdomyoma Disease
Rhabdomyosarcomas Disease
Ectomesenchymoma Disease
Paediatric gastrointestinal stromal tumour Disease
Schwannoma Disease
Neurofibroma Disease
Perineurioma Disease
Hybrid nerve sheath tumour Disease
Granular cell tumour Disease
Solitary circumscribed neuroma Disease
Ectopic meningioma and meningothelial hamartoma Disease
Benign triton tumour / neuromuscular choristoma Disease
Malignant peripheral nerve sheath tumour Disease
Intramuscular/juxta-articular myxoma Disease
Superficial angiomyxoma Disease
Deep angiomyxoma Disease
Angiomatoid fibrous histiocytoma Disease
Clear cell sarcoma of soft tissue Disease
Alveolar soft part sarcoma Disease
Extrarenal rhabdoid tumour Disease
PEComa Disease
Synovial sarcoma Disease
Epithelioid sarcoma Disease
Myoepithelial tumours of soft tissue Disease
Phosphaturic mesenchymal tumour Disease
Desmoplastic small round cell tumour Disease
Undifferentiated sarcomas Disease
Ewing sarcoma Disease
Round cell sarcoma with EWSR1::non-ETS fusions Disease
CIC-rearranged sarcoma Disease
Sarcoma with BCOR genetic alterations Disease
Subungual exostosis Disease
Bizarre parosteal osteochondromatous proliferation Disease
Osteoblastoma Disease
Osteoid osteoma Disease
Chondromesenchymal hamartoma of the chest wall Disease
Osteosarcoma Disease
Chondroblastoma Disease
Osteochondroma Disease
Chondromyxoid fibroma Disease
Enchondroma and enchondromatosis Disease
Chondrosarcoma Disease
Mesenchymal chondrosarcoma Disease
Vascular tumours of bone Disease
Aneurysmal bone cyst Disease
Giant cell tumour of bone Disease
Non-ossifying fibroma Disease
Notochordal tumours Disease
Simple bone cyst Disease
Adamantinoma Disease
Osteofibrous dysplasia Disease
Fibrous dysplasia Disease

CHAPTER 7 (GERM CELL TUMOURS)
Intratubular germ cell neoplasia (male gonadal) Disease
Gonadoblastoma Disease
Germinoma/dysgerminoma/seminoma Disease
Mature cystic teratoma Disease
Extragonadal teratoma Disease
Monodermal teratomas (female gonadal) Disease
Immature teratoma (female gonadal) Disease
Prepubertal-type testicular teratoma Disease
Postpubertal-type teratoma Disease
Embryonal carcinoma Disease
Yolk sac tumour Disease
Fetus in fetu Disease
Choriocarcinoma (non-gestational) Disease
Malignant mixed germ cell tumours Disease

CHAPTER 8 (RENAL AND MALE GENITAL TUMOURS)
Paediatric cystic nephroma Disease
Nephroblastoma Disease
Renal cell carcinoma with MiT translocations Disease
ALK-rearranged renal cell carcinoma Disease
Eosinophilic solid and cystic renal cell carcinoma Disease
SMARCB1-deficient renal medullary carcinoma Disease
Metanephric adenoma Disease
Metanephric adenofibroma Disease
Metanephric stromal tumour Disease
Ossifying renal tumour of infancy Disease
Mesoblastic nephroma Disease
Clear cell sarcoma of the kidney Disease
Malignant rhabdoid tumour of the kidney Disease
Anaplastic sarcoma of the kidney Disease
Renal Ewing sarcoma Disease
Juvenile granulosa cell tumour of the testis Disease

CHAPTER 9 (FEMALE GENITAL TUMOURS)
Ovarian fibroma Disease
Sclerosing stromal tumour Disease
Juvenile granulosa cell tumour of the ovary Disease
Sex cord tumour with annular tubules Disease
Papillary cystadenoma Disease
Sertoli-Leydig cell tumour Disease
Gynandroblastoma Disease
Small cell carcinoma of the ovary, hypercalcaemic type Disease
Mesonephric remnants and hyperplasia Disease
Mullerian papilloma Disease
Condyloma acuminatum Disease
Peritoneal inclusion cysts Disease

CHAPTER 10 (BREAST TUMOURS)
Fibroepithelial tumours Disease
Juvenile fibroadenoma Disease
Juvenile papillomatosis Disease

CHAPTER 11 (DIGESTIVE SYSTEM TUMOURS)
Hepatoblastoma Disease
Fibrolamellar variant of hepatocellular carcinoma Disease
Paediatric hepatocellular carcinoma Disease
Mesenchymal hamartoma Disease
Calcifying nested stromal-epithelial tumour Disease
Embryonal sarcoma of the liver Disease
Hepatic congenital haemangioma Disease
Hepatic infantile haemangioma Disease
Hepatic angiosarcoma Disease
Pancreatoblastoma Disease
Pancreatic acinar cell carcinoma Disease
Solid pseudopapillary neoplasm Disease
Gastroblastoma Disease
Appendiceal neuroendocrine tumours Disease

CHAPTER 12 (ENDOCRINE TUMOURS)
Follicular adenoma of the thyroid Disease
Papillary thyroid carcinoma Disease
Medullary thyroid carcinoma Disease
Spindle epithelial tumour with thymus-like elements Disease
Parathyroid adenoma Disease
Adrenal cortical tumours Disease
Sympathetic paraganglioma Disease
Parasympathetic paraganglioma (head and neck paraganglioma) Disease
Phaeochromocytoma Disease
Composite phaeochromocytoma/paraganglioma Disease
Other neuroendocrine tumours Disease

CHAPTER 13 (HEAD AND NECK TUMOURS)
Squamous cell papilloma of the larynx Disease
White sponge naevus Disease
Congenital granular cell epulis Disease
Central giant cell granuloma Disease
Odontogenic tumours Disease
Ossifying fibroma Disease
Sinonasal tract myxoma Disease
Nasal dermoid cyst Disease
Nasopharyngeal dermoid Disease
Sinonasal chondromesenchymal hamartoma Disease
Pleomorphic adenoma Disease
Mucoepidermoid carcinoma Disease
Acinic cell carcinoma Disease
Sialoblastoma Disease
Nasopharyngeal carcinoma Disease
NUT carcinoma Disease
Melanotic neuroectodermal tumour of infancy Disease

CHAPTER 14 (THORACIC TUMOURS)
Fetal lung interstitial tumour Disease
Congenital peribronchial myofibroblastic tumour Disease
Pleuropulmonary blastoma Disease
Cardiac rhabdomyoma Disease

CHAPTER 15 (SKIN TUMOURS)
Hamartomas Disease
Angiokeratoma Disease
Epidermal naevi Disease
Pilomatricoma Disease
Congenital naevi Disease
Junctional, compound, and dermal naevi Disease
Blue naevus Disease
Spitz naevus Disease
Pigmented spindle cell naevus (Reed naevus) Disease
Melanoma Disease

CHAPTER 16 (GENETIC TUMOUR SYNDROMES)
Neurofibromatosis type 1 Disease See GTS5 volunteer sheet for authorship status N/A N/A N/A N/A N/A N/A N/A
Neurofibromatosis type 2 Disease See GTS5 volunteer sheet for authorship status N/A N/A N/A N/A N/A N/A N/A
Tuberous sclerosis Disease
Naevoid basal cell carcinoma syndrome (Gorlin syndrome) Disease
Retinoblastoma syndrome Disease
Von Hippel-Lindau syndrome Disease See GTS5 volunteer sheet for authorship status N/A N/A N/A N/A N/A N/A N/A
Hereditary phaeochromocytoma-paraganglioma syndromes Disease
WAGR syndrome Disease See GTS5 volunteer sheet for authorship status N/A N/A N/A N/A N/A N/A N/A
Beckwith-Wiedemann and related overgrowth syndromes Disease
Familial adenomatous polyposis Disease See GTS5 volunteer sheet for authorship status N/A N/A N/A N/A N/A N/A N/A
Lynch syndrome Disease See GTS5 volunteer sheet for authorship status N/A N/A N/A N/A N/A N/A N/A
Xeroderma pigmentosum Disease
Rothmund-Thomson syndrome Disease
Li-Fraumeni syndrome Disease See GTS5 volunteer sheet for authorship status N/A N/A N/A N/A N/A N/A N/A
DICER1 syndrome Disease See GTS5 volunteer sheet for authorship status N/A N/A N/A N/A N/A N/A N/A
BAP1 tumour predisposition syndrome Disease
Constitutional mismatch repair deficiency syndrome Disease See GTS5 volunteer sheet for authorship status N/A N/A N/A N/A N/A N/A N/A
Rhabdoid tumour predisposition syndrome Disease
Retrieved from "https://ccga.io/index.php?title=PEDS5:Volunteer_Assignments_and_Opportunities&oldid=15425"