Blog Archive

Wednesday, September 8, 2021

09-08-2021-1739 - Trinity Fields - Deathstars



above. Deathstars - Trinity Fields 

Marilyn Manson - Cry Little Sister


090820211738 

09-08-2021-1724 - 2653/4-5,6

 09-08-2021-1724 - 2653/4-5,6

Led Zeppelin - Mothership (Full Album) (2007 Remaster) | Led Zeppelin - ...


090820211659

When the Levee Breaks (Remaster) - led zeppelin


090820211607

Sir Mix-A-Lot - Baby Got Back (Official Music Video)


0908020211525

09-08-2021-1518 - Oxyphilic Adenocarcinoma Follicule oncocytic hurthle cell Thyroid endocrine endocrinology adeno SEER & PUBMED Process "...abundant granular eosinophilic cytoplasm (oncocytes)."

 Oxyphilic Adenocarcinoma

MedGen UID: 
61427
 •Concept ID: 
C0205642
 •
Neoplastic Process
Synonyms:Adenocarcinoma, Oxyphilic; Adenocarcinomas, Oxyphilic; Oxyphilic Adenocarcinomas
SNOMED CT: Follicular carcinoma, oxyphilic cell (57596004); Oxyphilic adenocarcinoma (443261008); Oxyphilic adenocarcinoma (57596004); Oncocytic carcinoma (57596004); Oncocytic adenocarcinoma (57596004); Hurthle cell carcinoma (57596004); Hurthle cell adenocarcinoma (57596004)

Definition

An adenocarcinoma characterized by the presence of large malignant epithelial cells with abundant granular eosinophilic cytoplasm (oncocytes). Representative examples include thyroid gland oncocytic follicular carcinoma, oncocytic breast carcinoma, and salivary gland oncocytic carcinoma. [from NCI]
https://www.ncbi.nlm.nih.gov/medgen/61427

 https://seer.cancer.gov/icd-o-3/sitetype.icdo3.20210607.pdf#search=plasma%20cell

09-08-2021-1517 - Myelodysplastic/Myeloproliferative neoplasm, unclassifiable IMMUNOPROLIFERATIVE DISEASES reticular reticulum reticulus endoplasmic reticulum mitochondria cell SEER

 NEOPLASMS OF HISTIOCYTES AND ACCESSORY LYMPHOID CELLS IMMUNOPROLIFERATIVE DISEASES

PRECURSOR LYMPHOID NEOPLASMS

LYMPHOID LEUKEMIA, NOS PROLYMPH/PRECURS LEUKEMIA

CHRONIC MYELOPROLIFERATIVE DIS. MYELOPLASTIC/MYELOPROLIFERATIVE NEOPLASMS

975 9759/3 976 9766/3 981 9811/3

Fibroblastic reticular cell tumor Lymphomatoid granulomatosis, grade 3
B lymphoblastic leukemia/lymphoma, NOS

982 9823/3

Chronic lymphocytic leukemia/small lymphocytic lymphoma

9812/3 Leukemia/lymphoma with t(9;22)(q34;q11.2);BCR-ABL1
9813/3 Leukemia/lymphoma with t(v;11q23);MLL rearranged
9814/3 Leukemia/lymphoma with t(12;21)(p13;q22);TEL-AML1(ETV6-RUNX1) 9815/3 B lymphoblastic leukemia/lymphoma with hyperdiploidy
9816/3 Leukemia/lymphoma with hypodiploidy (hypodiploid ALL)
9817/3 B lymphblastic leukemia/lymphoma with t(5;14)(q31;q32);IL3-IGH 9818/3 Leukemia/lymphoma with t(1;19)(q23;p13.3); E2A PBX1 (TCF3 PBX1) 9819/3 B-lymphocytic leukemia/lymphoma, BCR-ABL1-like

T-cell large granular lymphocytic leukemia

983 9831/3
9837/3 T lymphoblastic leukemia/lymphoma

996 9965/3
9967/3 Myeloid and lymphoid neoplasm with FGFR1 abnormalities

Myeloid and lymphoid neoplasms with PDGFRB rearrangement

997 9971/3
9975/3 Myelodysplastic/Myeloproliferative neoplasm, unclassifiable

https://seer.cancer.gov/icd-o-3/sitetype.icdo3.20210607.pdf#search=plasma%20cell



Above. Lil Jon & The East Side Boyz - Get Low

09-08-2021-1515 - SEER Validation List https://seer.cancer.gov/icd-o-3/sitetype.icdo3.20210607.pdf#search=plasma%20cell Muller FBI & Friends



https://seer.cancer.gov/icd-o-3/sitetype.icdo3.20210607.pdf#search=plasma%20cell






(Repost, Original Post Present)

08-24-2021-1053 - Anemia - Autoimmune hemolytic anemia - The term "macrocytic" refers to the enlarged size of the red blood cells.



Autoimmune hemolytic anemia

Anemia (NOS) is a decrease in the number of red blood cells. Many cancer patients develop anemia due to the cancer and/or cancer therapy. This condition may be referred to as Anemia in neoplastic disease or anemia of chronic disorders. The anemia by itself is not reportable. The neoplasm causing the anemia would be reportable.

Aplastic anemia occurs when the bone marrow does not make enough new red cells. A neoplasm may cause the aplastic anemia; however, the aplastic anemia by itself is not reportable. (See also pancytopenia)

Hemolytic (autoimmune) anemia is a group of acute or chronic anemias, inherited or acquired, characterized by shortened survival of mature erythrocytes and inability of bone marrow to compensate for the decreased life span.

Idiopathic refractory anemia is when the cause of the anemia is not known. This is not the same thing as Refractory Anemia(9980/3).

Iron -refractory iron deficiency anemia (IRIDA) or refractory iron deficiency anemia is an autosomal recessive disorder.

Macrocytic anemia is usually caused by vitamin deficiencies, alcohol use, medications or thyroid. The term "macrocytic" refers to the enlarged size of the red blood cells.
Anemia
https://seer.cancer.gov/seertools/hemelymph/532b32a0e4b0626b1926e990/


The term "macrocytic" refers to the enlarged size of the red blood cells.


https://seer.cancer.gov/icd-o-3/sitetype.icdo3.20210607.pdf#search=plasma%20cell


ML, SMALL B-CELL LYMPHOCYTIC


PRECURS. CELL LYMPHOBLASTIC LYMPH.


PLASMA CELL TUMORS


SQUAMOUS CELL CARCINOMA, NOS


GIANT & SPINDLE CELL CARCINOMA


BRONCHIOLO-ALVEOLAR ADENOCA.


CLEAR CELL ADENOCARCINOMA, NOS


ACINAR CELL CARCINOMA


FIBROMATOUS NEOPLASMS


SARCOMA, NOS RHABDOMYOSARCOMA, NOS


EMBRYONAL RHABDOMYOSARCOMA MIXED TUMOR, MALIGNANT, NOS


ML, LARGE B-CELL, DIFFUSE


FOLLIC. & MARGINAL LYMPH, NOS


IMMUNOPROLIFERATIVE DISEASES


LYMPHOID LEUKEMIA, NOS PROLYMPH/PRECURS LEUKEMIA

CHRONIC MYELOPROLIFERATIVE DIS.


OXYPHILIC ADENOCARCINOMA


DUCT CARCINOMA
ACINAR CELL CARCINOMA ADENOSQUAMOUS CARCINOMA


ADENOCA. WITH METAPLASIA


SARCOMA, NOS

FIBROMATOUS NEOPLASMS

SARCOMA, NOS MYXOSARCOMA LIPOSARCOMA NEOPLASMS


MYOMATOUS NEOPLASMS

RHABDOMYOSARCOMA, NOS


MIXED TUMOR, MALIGNANT, NOS CARCINOSARCOMA, NOS

MESENCHYMOMA, MALIGNANT


ML, SMALL B-CELL LYMPHOCYTIC

ML, LARGE B-CELL, DIFFUSE

granuloma sarcoma lymphoma


immunoblastic


FOLLIC. & MARGINAL LYMPH, NOS




NEOPLASMS OF HISTIOCYTES AND ACCESSORY LYMPHOID CELLS


IMMUNOPROLIFERATIVE DISEASES

PRECURSOR LYMPHOID NEOPLASMS


MAL. MEL. IN JUNCT. NEVUS


MAL. MELAN. IN GIANT PIGMT. NEVUS


CLEAR CELL ADENOCARCINOMA, NOS MUCOEPIDERMOID CARCINOMA MUCINOUS ADENOCARCINOMA


PAPILLARY ADENOCARCINOMA, NOS


Lymphomatoid granulomatosis, grade 3


Marginal zone B-cell lymphoma, NOS

8693/3 Extra-adrenal paraganglioma, malignant


MEDIASTINUM C381-C383,C388

THYMUS C379


PLEURA C384


RESPIRATORY,NOS C390,C398-C399


9690/3 Follicular lymphoma, NOS
9691/3 Follicular lymphoma, grade 2
9695/3 Follicular lymphoma, grade 1
9698/3 Follicular lymphoma, grade 3
9699/3 Marginal zone B-cell lymphoma, NOS


BONES & JOINTS (EXCL SKULL AND FACE, MANDIBLE) C400-C403,C408-C409,C412-C414,C418-C419 Dr. Layng Getting Some Brown Right


BLOOD, BONE MARROW, & HEMATOPOIETICSYS C420, C421, C424


FOLLIC. & MARGINAL LYMPH, NOS 969


Acute myelomonocytic leukemia



RETICULO-ENDOTHELIAL C423


Langerhans cell histiocytosis, disseminated


SPLEEN C422

Skin

Peripheral Nerves

Retroperitoneum

(Metastatic proc BK Study USA match)


RETROPERITONEUM & PERITONEUM C480-C482,C488


CONNECTIVE & SOFT TISSUE C490-C496,C498-C499


VAGINA & LABIA C510-C512,C518, C529 (AI or NAI)


CERVIX UTERI C530-C531,C538-C539


CORPUS UTERI C540-C543,C548-C549


UTERUS, NOS C559


OVARY C569


PRECURS. CELL LYMPHOBLASTIC LYMPH.

PLASMA CELL TUMORS

MAST CELL TUMORS


FALLOPIANTUBE C570


OTHER FEMALE GENITAL (EXCL FALLOPIAN TUBE) C571-C574,C577-C579


PLACENTA C589


MULLERIAN MIXED TUMOR


KIDNEY C649


RENAL PELVIS, URETER C659, C669


URINARYBLADDER C670-C679


OTHER URINARYORGANS C680-C681,C688-C689


ORBIT & LACRIMALGLAND, (EXCL. RETINA, EYE, NOS) C690-C691, C693, C695-C698


RETINA C692 - winner nikiya @ nlab


EYEBALL C694


EYE, NOS C699


MENINGES (CEREBRAL,SPINAL) C700-C701,C709


BRAIN, & CRANIAL NERVES, & SPINAL CORD, (EXCL. VENTRICLE, CEREBELLUM) C710-C714, C717-C719, C720-C725


VENTRICLE C715


CEREBELLUM C716


OTHER NERVOUS SYSTEM C728-C729


THYROID GLAND C739


ADRENALGLANDS C740-C741,C749


PARATHYROIDGLAND C750


PITUITARYGLAND C751


CRANIOPHARYNGEALDUCT C752


PINEAL GLAND C753


ICD-0-3 SEER SITE/HISTOLOGY VALIDATION LIST OTHER ENDOCRINE GLANDS C754-C755,C758-C759


ILL-DEFINED C760-C768


LYMPH NODES C770-C775,C778-C779


UNKNOWN C809

N/A 900

https://seer.cancer.gov/icd-o-3/sitetype.icdo3.20210607.pdf#search=plasma%20cell

above. Right Thurr chingy

Dmitri Shostakovich - Waltz No.2 ( One hour version )


090820211507

09-08-2021-1008 - 1. Gas phase (tissue cell expansion by gas collection; nitrogen, voc, protein, virus) 2. fibroti scar inflammation post granulocyte infiltration 3. seppage and holleing with voc agglomerate (dysplasia proliferative granulomatosis cancotics virus gas induction by voc exposure inflam wound heal fibrotics scar deformation gen mod chrom transl/disl/etc. dna cystu w/ gas nuc rad heavy met etc. biofilm plaque tartar calculus mineralization liquefication)

Wednesday, September 8, 2021

09-08-2021-0937 - Primary myelofibrosis (PMF) is a rare bone marrow blood cancer.[1] ' This is most often associated with a somatic mutation in the JAK2, CALR, or MPL gene markers. In PMF, the healthy marrow is replaced by scar tissue (fibrosis), '

 Primary myelofibrosis (PMF) is a rare bone marrow blood cancer.[1] It is classified by the World Health Organization (WHO) as a type of myeloproliferative neoplasm, a group of cancers in which there is growth of abnormal cells in the bone marrowThis is most often associated with a somatic mutation in the JAK2, CALR, or MPL gene markers. In PMF, the healthy marrow is replaced by scar tissue (fibrosis), resulting in a lack of production of normal blood cells. Symptoms include anemia, increased infection and an enlarged spleen (splenomegaly).

In 2016, prefibrotic primary myelofibrosis was formally classified as a distinct condition that progresses to overt PMF in many patients, the primary diagnostic difference being the grade of fibrosis.[2]

Primary myelofibrosis
Other namesPMF, Overt PMF, Myelofibrosis
SpecialtyOncology and Hematology

https://en.wikipedia.org/wiki/Primary_myelofibrosis 



Women in combat: Test failures raise questions about how many can succeed -  Washington Times

Arrhythmogenic cardiomyopathy
Other namesarrhythmogenic right ventricular cardiomyopathy (ARVC), arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C), right ventricular dysplasia
Arrhythmogenic right ventricular cardiomyopathy - histology.jpg
Typical micro-histologic features of ARVC/D. Ongoing myocyte death (upper) with early fibrosis and adipocyte infiltration (lower).
SpecialtyCardiology 
https://en.wikipedia.org/wiki/Arrhythmogenic_cardiomyopathy


1. Gas phase (tissue cell expansion by gas collection; nitrogen, voc, protein, virus)
2. fibroti scar inflammation post granulocyte infiltration
3. seppage and holleing with voc agglomerate



Above. Flo Rida (ft. T-Pain) - Low


09-08-2021-0953 - tumor or dysplasia agglomeration or proliferation small capillary tumor/deformity and blood vessel tumor/deformity - NLAB

Cell proliferation metastatic dysplasia

tumor or dysplasia agglomeration or proliferation

small capillary tumor and blood vessel tumor/deformity

small cell tumor

biofilm tumor

myx xy yxo

Last gen dis, met dis conde, immunosuppr, leukemia/cancer (dysplasia proliferative granulation dysfunction degen etc. matricing widening

cell proliferation metastatic dysplasia adeno

STD CL1 Syphalli, not agranulolytic. granulation disseminative granulation/granulomatoseous (Granulomatosis ) inflammation dna cystulation cystular fibrotics fibromatotics fibrotics sarcotikxs, etc..

Anticipation to CVD,

Granuloma Annulare Lupus erythematosus systemic Lyme Disease Autoimmune Disease

Blood vessel tumor, disseminated vascular lining tumor, shear/frictionated interspace

syphalli type 2, irradiation dec, syncytin, matricing error decom




Women in combat: Test failures raise questions about how many can succeed -  Washington Times
Fridrihs Ketlers.jpg


Arrhythmogenic cardiomyopathy
Other namesarrhythmogenic right ventricular cardiomyopathy (ARVC), arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C), right ventricular dysplasia
Arrhythmogenic right ventricular cardiomyopathy - histology.jpg
Typical micro-histologic features of ARVC/D. Ongoing myocyte death (upper) with early fibrosis and adipocyte infiltration (lower).
SpecialtyCardiology 
https://en.wikipedia.org/wiki/Arrhythmogenic_cardiomyopathy

1. Gas phase (tissue cell expansion by gas collection; nitrogen, voc, protein, virus)
2. fibroti scar inflammation post granulocyte infiltration
3. seppage and holleing with voc agglomerate




Above. Yung Joc - It's Goin' Down (feat. Nitti)


09-08-2021-0949 - Segmental arterial mediolysis (SAM)

 Segmental arterial mediolysis (SAM) is a rare disorder of the arteries characterized by the development of aneurysms, blood clots, narrowing of the arteries (stenoses), and blood collections (hematomas) in the affected distribution.[1][2]

SAM most commonly affects the arteries supplying the intestines and abdominal organs.[citation needed]

https://en.wikipedia.org/wiki/Segmental_arterial_mediolysis





Above. 

Ricky Martin - Livin' La Vida Loca (Lyrics)

09-08-2021-0948 - Laparotomy for visceral ischemia and gangrene

Am Surg
. 2007 Oct;73(10):1006-8.
Laparotomy for visceral ischemia and gangrene
Karen Woo 1, Kevin Major, Som Kohanzadeh, Alexander D Allins
Affiliations expand
PMID: 17983069
https://pubmed.ncbi.nlm.nih.gov/17983069/


above. Gold Digger kanye west

09-08-2021-0948 - 2640/1-2,3

 09-08-2021-0948 - 2640/1-2,3

09-08-2021-0947 - Lipofibromatosis-like neural tumor (LPF-NT) lipo fibro matosis fibromatosis fibrosis cancer tumor lipoma

 Lipofibromatosis-like neural tumor (LPF-NT) is an extremely rare soft tissue tumor first described by Agaram et al in 2016.[1] As of mid-2021, at least 39 cases of LPF-NT have been reported in the literature.[2][3][4][5] LPF-NT tumors have several features that resemble lipofibromatosis (LPF) tumors,[6] malignant peripheral nerve sheath tumors, spindle cell sarcomas,[3] low-grade neural tumors, peripheral nerve sheath tumors, and other less clearly defined tumors;[1] Prior to the Agaram at al report, LPF-NTs were likely diagnosed as variants or atypical forms of these tumors. The analyses of Agaram at al and subsequent studies[4] uncovered critical differences between LPF-NT and the other tumor forms which suggest that it is a distinct tumor entity differing not only from lipofibromatosis but also the other tumor forms.[7]

LPF-NTs are locally invasive, are commonly treated by surgical excision, and have a relatively high rate of local recurrence if their surgical excisions are incomplete.[8] They are generally considered to be benign, non-metastasizing(i.e. not spreading to other parts of the body) tumors.[6][8] However, one case of LFT-NT reported by Agaram et al was associated with metastasis, apparently as a result of the tumor's cells transformation into a malignant sarcoma. Further studies are needed to determine the frequency of such cases and the overall metastatic potential of LPF-NT.[1]

LPF-NTs were given the "neural tumor" terminology because in at least some cases: 1) their tumor cells express S100 and CD34 but not SOX10 proteins, a pattern that is often found in neural[7] and neuroectodermal tumor cells;[1] and 2) their histopathology consists of tumor cell infiltrations into adipose tissues in a pattern that is very similar to that found in some low grade malignant peripheral nerve sheath tumors.[1]

https://en.wikipedia.org/wiki/Lipofibromatosis-like_neural_tumor




Above. M.I.A. - Paper Planes

09-08-2021-0945 - Fibromuscular dysplasia (FMD)

 Fibromuscular dysplasia (FMD) is a non-atherosclerotic, non-inflammatory disease of the blood vessels that causes abnormal growth within the wall of an artery.[1] FMD has been found in nearly every arterial bed in the body although the most common arteries affected are the renal and carotid arteries.[1][2][3]

There are various types of FMD, with multi-focal fibroplasia being the most common. Further, less common, forms of the disease include focal (previously known as intimal) and adventitial fibroplasia.[1][2][3][4] FMD predominantly affects middle-aged women, but has been found in men and people of all ages.[1] Pediatric cases of FMD are vastly different from that of the adult population, and poorly studied. The prevalence of FMD is not known and, although the disease was initially thought to be rare, some studies have suggested that it may be underdiagnosed.[5]

Fibromuscular dysplasia
Fibr.jpg
The "string-of-beads" feature in multi-focal fibromuscular dysplasia. The sign is caused by areas of relative stenoses alternating with small aneurysms.
SpecialtyCardiology 

https://en.wikipedia.org/wiki/Fibromuscular_dysplasia



above. Maneater Nelly Furtado

09-08-2021-0942 - Acute myeloid leukemia with mutated RUNX1

 

Acute myeloid leukemia with mutated RUNX1
https://seer.cancer.gov/seertools/hemelymph/5a7e288d1ef557f9c8636d31/
myeloproliferative neoplasa
https://seer.cancer.gov/seertools/hemelymph/51f6cf57e3e27c3994bd5387/
https://www.hopkinsmedicine.org/hematology/mpd/definitions

dysplasia proliferative agglomerate granulocyte


above. 

Michael Jackson - Billie Jean (Official Video)

09-08-2021-0939 - Extramedullary hematopoiesis (EMH or sometimes EH) hematopoiesis occurring outside of the medulla of the bone (bone marrow).[2] It can be physiologic or pathologic.

 Extramedullary hematopoiesis (EMH or sometimes EH[1]) refers to hematopoiesis occurring outside of the medulla of the bone (bone marrow).[2] It can be physiologic or pathologic. 

Physiologic EMH occurs during embryonic and fetal development; during this time the main site of fetal hematopoiesis are liver and the spleen.

Pathologic EMH can occur during adulthood when physiologic hematopoiesis can't work properly in the bone marrow and the hematopoietic stem cells (HSC) have to migrate to other tissues in order to continue with the formation of blood cellular components. Pathologic EMH can be caused by myelofibrosis,[3] thalassemias or disorders caused in the hematopoietic system.

Physiologic EMH[edit]

During fetal development, hematopoiesis occurs mainly in the fetal liver and in the spleen followed by localization to the bone marrow.[4] Hematopoiesis also takes place in many other tissues or organs such as the yolk sac, the aorta-gonad mesonephros (AGM) region, the spleen, and lymph nodes. During development, vertebrates go through a primitive and a definitive phase of hematopoiesis. The lungs also play a role in platelet production in adults.[5]

Primitive hematopoiesis[edit]

Primitive hematopoiesis occurs in the yolk sac during early embryonic development. It is characterized by the production of erythroid progenitors or nucleated erythrocytes, also known as erythroblasts or megaloblasts. The main objective of the production of these cells will be the facilitation of tissue oxygenation to support rapid embryonic growth. This primitive phase is transitory and the cells that are produced express embryonic globins, aren't pluripotent, and aren't capable of self-renewal.

Definitive hematopoiesis[edit]

Definitive hematopoiesis differs from the primitive phase through the production of hematopoietic stem cells. The formation of these cells occurs in the AGM later in development. Later, they migrate to the fetal liver where the majority of physiologic EMH takes place. Finally, once the bone marrow has developed, they migrate there. They can also migrate to the spleen and lymph nodes where hematopoiesis can occur, but to a lesser degree.

Pulmonary hematopoiesis[edit]

Pulmonary hematopoiesis also appears to play an important role in adults.[5] In comparison to the bone marrow, where trilineage hematopoiesis occurs, the lungs preferentially contribute to the production of platelets through a resident population of megakaryocytes. This is supported by studies showing that blood leaving the lungs has more platelets and fewer progenitor cells than blood entering the lungs. It has been seen that in cases of severe thrombocytopenia, pulmonary megakaryocytes migrate out of lungs into the bone marrow, where they help to replenish the depleted bone marrow population.


https://en.wikipedia.org/wiki/Extramedullary_hematopoiesis



above. 

Ginuwine - Pony

09-08-2021-0938 - Myeloproliferative neoplasms (MPNs)

Myeloproliferative neoplasms (MPNs) are a group of rare blood cancers in which excess red blood cellswhite blood cells or platelets are produced in the bone marrow.  Myelo refers to the bone marrowproliferativedescribes the rapid growth of blood cells and neoplasm describes that growth as abnormal and uncontrolled.

The overproduction of blood cells is often associated with a somatic mutation, for example in the JAK2CALR, TET2, and MPL gene markers.

In rare cases, some MPNs such as primary myelofibrosis may accelerate and turn into acute myeloid leukemia.[1] 

Myeloproliferative neoplasm
Other namesMyeloproliferative diseases (MPDs)
Myelogram of person with a myeloproliferative disorder.png
Myelogram of someone with a myeloproliferative disorder.
SpecialtyHematology and oncology

https://en.wikipedia.org/wiki/Myeloproliferative_neoplasm


above. 

Christina Aguilera - Dirrty (VIDEO) ft. Redman