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The surgical approach depends on the tumor location and how much surrounding tissue was removed. For an area of skin that isn’t too deep, doctors may use a skin graft, or a small portion of the top layers of healthy skin. It’s usually taken from an area of your body where missing skin wouldn’t be noticeable, such as the inner thigh.

To fill in and close a larger or deeper opening of the skin, doctors may use a local flap, or a piece of nearby skin, which can include underlying fat and muscle. It is moved while it’s still attached to its current blood supply. Cartilage, the firm, white tissue that helps give structure to parts of the body such as the ears and nose, may also need to be moved during reconstruction.

Skin flaps are often left in place for several weeks as the surgical site heals. In a second surgery, they are contoured to match the appearance of the surrounding healthy skin and tissues. For example, areas of the nose can be repaired with a local skin flap from the cheek and cartilage from the ear. Doctors perform another surgery to remove any extra flap tissue and carefully reconstruct the shape of the nose with minimal scarring to the face.

Sometimes, if a large skin cancer needs to be removed, doctors may use free flaps of skin, fat, or muscle from a distant part of the body, such as the back or abdomen, to fill in areas where the cancer has been removed. These tissue flaps are called “free” because they are detached from their blood supply. Blood vessels are reattached at the site of repair.

After surgery, our doctors help scars heal properly. For example, they can carefully tape incisions after surgery and leave this tape in place for several days, to prevent scarring. If a scar becomes raised or red, doctors can inject the area with steroids, which helps flatten the tissue and remove the redness. Lasers can also treat discoloration.

Recovery time from basal and squamous cell cancer surgery varies, depending on the size of the tumor, whether lymph nodes were removed, and whether you undergo reconstruction.

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Perlmutter Cancer Center specialists provide care and support during treatment.

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Light Sources SIG

(formerly Synchrotron Radiation)

Officers

Chair 2018

Pawel Grochulski

Canadian Light Source

Univ. of Saskatchewan

101 Perimeter Rd

Saskatoon SK S7N0X4

Canada

pawel.grochulski@lightsource.ca

Chair-elect 2018/Chair 2019

Ray Sierra

SLAC Stanford Univ.

2575 Sand Hill Rd MS 59

Menlo Park, CA 94025

rsierra@slac.stanford.edu

Past Chair

Allen Orville

Diamond Light Source

Diamond House

Harwell Science and Innovation Campus

Didcot, Oxfordshire

OX11 0DE

United Kingdom

allen.orville@diamond.ac.uk

Annual Reports

Annual reports contain information on the activities of the SIG for the year, issues addressed by the SIG members, future activity planning and any changes to the operations or constitution of the SIG.

2017 Report Download

2016 Report Download

2015 Report Download

2014 Report Download

2013 Report Download

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2010 Report Download

2009 Report Download

Constitution

(With amendments ratified December 2006 December 2013)

I.NAME: The name of this group shall be The SCIENTIFIC INTEREST GROUP on Light Sources (formerly) Synchrotron Radiation.

II.PURPOSE: The purpose of this group of the American Crystallographic Association (hereafter ACA) is to further the advancement of all aspects of synchrotron x-ray research and to promote communication between persons interested in such techniques and results.

III.RELATIONSHIP TO THE AMERICAN CRYSTALLOGRAPHIC ASSOCIATION: The constitution of this organization shall be consistent with the Constitution, By-laws, and Operating Rules of the ACA. In the event of conflict the Constitution, By-laws and Rules of the ACA shall prevail.

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A nine-month stint with The Associated Press brought Sandra to Detroit…27years ago. She has a bachelor’s in journalism and history from Indiana University, and along the wayadded twomaster’s degrees, one in library and information science and another in public administration, both from Wayne State University. Sandra has worked forThe (Toledo) Blade covering education/children’s issues,Detroit’s Metro Times and FEMA , where she deployed to Louisiana to help coordinate/communicate about community rebuilding/planning efforts for/after disasters. Sandra haswon awards for broadcast, print, digital and community engagement workfrom the Michigan Associated Press, the Michigan Association of Broadcasters,Association of Alternative Newsweeklies, State Bar of Michigan, Michigan Press Association and Society of Professional Journalists-Detroit chapter. WSU ’s Public Administration program named her Alum of the Year in 2015 for her WDET work covering Detroit’s bankruptcy. Sandra teaches adjunct faculty at Wayne State (political science)and UM -Dearborn (graduate public administration program). She volunteers with Big Brothers/Big Sisters of Metropolitan Detroit and with Freedom House Detroit . She loves her husband, dog, bicycle, usually in that order. Find her sailing on the Detroit River in her sparetime.

@WDETSandra

March 21, 2018

The new federal tax plan has a program to steer development to poor neighborhoods. State officials are not designing it that way, Bridgereports.

March 6, 2018

Mayor Duggan gives his 2018 address. Listen at 101.9 FM , watch ithere.

Jan. 19, 2018 on CultureShift

What will the term-limited Snyder say in his last State of the Stateaddress?

Jan. 9, 2018

Three casinos report paying $113 million to city, Detroit’s third largest revenuesource.

Dec. 28, 2017

A WDET analysis helps you understand how to get records and documents from yourmunicipality.

Dec. 27, 2017

Governmental transparency advocate lobbies to guarantee access to governor, legislature’s publicrecords.

The information that is really helpful for the public to know often is really difficult toget.”

QMUL Directory

I am interested in understanding how cancer cells ‘switch off’ the normal immune response in acute myeloid leukaemia with the aim of developing novel immunotherapeutic strategies.

I am currently developing several research projects:

I started work in the Haemato-Oncology department in the Barts Cancer Institute in October 2011 as part of John Gribben’s cancer immunotherapy group. I developed my research interests as an MRC Clinical Training Fellow in the group between 2005 and 2009 when I investigated T cells in acute myeloid leukaemia. I gained experience in immunomagnetic cell separation, flow cytometry, gene expression profiling and confocal microscopy of the immune synapse.

I developed a technique for separating T cells from the peripheral blood of patients presenting with AML that was published in the Journal of Immunological Methods in 2009 and my data characterising T cell defects in AML was published in Blood in the same year. I left Barts in 2009 to complete my clinical haematology training which included a year spent at the Hammersmith Hospital as a stem cell transplant coordinator. During this time, I gained valuable experience in the organisation as well as inpatient and outpatient management of patients undergoing allogeneic stem cell transplantation.

I now plan to develop as an independent researcher taking forward my basic science research examining T cell function in haematologic malignancy to investigate new immunotherapeutic strategies in AML.

Peripheral blood T cells in acute myeloid leukemia (AML) patients at diagnosis have abnormal phenotype and genotype and form defective immune synapses with AML blasts. Le Dieu R, Taussig D, Ramsay AG, Mitter R, Lee AM, Lister TA, Gribben JG. Blood 2009 Oct; 114 (18): 3909-16 PMID: 19710498

Array-based DNA methylation profiling in follicular lymphoma. O’Riain C, O’Shea DM, Yang Y, Le Dieu R, Gribben JG, Summers K, Yeboah-Afari J, Bhaw-Rosen L, Fleischmann C, Mein CA, Crook T, Smith P, Kelly G, Rosenwald A, Ott G, Campo E, Rimsza LM, Smeland EB, Chan WC, John son N, Gascoyne RD, Reimer S, Braziel RM, Wright GW, Staudt LM, Lister TA, Fitzgibbon J. Leukemia 2009 Oct; 23 (10): 1858-66 PMID: nike roshe run nm white wildflower 0DfaX6

Negative immunomagnetic selection of T cells from peripheral blood of presentation AML specimens. Le Dieu R, Taussig D, Lister TA, Gribben JG. Journal of Immunological Methods 2009 Aug ; 348 (1-2): 95-100 PMID: 19576900

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