{"id":14062,"date":"2018-01-05T11:50:32","date_gmt":"2018-01-05T18:50:32","guid":{"rendered":"https:\/\/www.uchealth.org\/today\/?p=14062"},"modified":"2025-04-15T11:55:46","modified_gmt":"2025-04-15T17:55:46","slug":"scleroderma","status":"publish","type":"post","link":"https:\/\/www.uchealth.org\/today\/scleroderma\/","title":{"rendered":"Scleroderma\u2019s threat is more than skin deep"},"content":{"rendered":"<div style=\"margin-top: 0px; margin-bottom: 0px;\" class=\"sharethis-inline-share-buttons\" ><\/div><p>Dr. Aryeh Fischer is a rheumatologist who is an expert in diagnosing and treating lung disease in patients with a condition that is too often associated only with the skin.<\/p>\n<figure id=\"attachment_14073\" aria-describedby=\"caption-attachment-14073\" style=\"width: 300px\" class=\"wp-caption alignright\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-14073 size-medium\" src=\"https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050507\/EXT_121917_Joy-Swimming.jpgsized.webp\" alt=\"A woman named Joy Matthews stands in a swimming pool with a floating beer cooler that protects her oxygen tank.\" width=\"300\" height=\"225\" srcset=\"https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050507\/EXT_121917_Joy-Swimming.jpgsized.webp 1200w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050507\/EXT_121917_Joy-Swimming.jpgsized-300x225.webp 300w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050507\/EXT_121917_Joy-Swimming.jpgsized-1024x768.webp 1024w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050507\/EXT_121917_Joy-Swimming.jpgsized-768x576.webp 768w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050507\/EXT_121917_Joy-Swimming.jpgsized-150x113.webp 150w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050507\/EXT_121917_Joy-Swimming.jpgsized-200x150.webp 200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><figcaption id=\"caption-attachment-14073\" class=\"wp-caption-text\">With the help of a floating beer cooler that protects her oxygen tank, Joy Mathews is back to swimming to slow the progression of her lung disease.<\/figcaption><\/figure>\n<p>If that sounds confusing, it\u2019s befitting of an autoimmune disorder that is not only rare and elusive but even misleadingly named: scleroderma. Its Greek origins suggest hardening of the skin, and indeed the condition does cause stiffening of connective tissue. But the damage is not confined to the skin, Fischer said.<\/p>\n<p>The more accurate term for the disease is systemic sclerosis (SSc), a term that reflects its potential to involve multiple organs throughout the body.<\/p>\n<p>\u201c\u2019Scleroderma\u2019 is a colloquial term,\u201d said Fischer, who practices at <a href=\"https:\/\/www.uchealth.org\/locations\/uchealth-university-of-colorado-hospital-uch\/\">UCHealth University of Colorado Hospital<\/a>. \u201cI\u2019m not a skin doctor.\u201d<\/p>\n<p>Instead, Fischer focuses much of his attention on diagnosing and treating <a href=\"https:\/\/www.uchealth.org\/diseases-conditions\/interstitial-lung-disease-ild\/\">interstitial lung disease<\/a> \u2013 scarring of the lungs that he said occurs in about three-quarters of the roughly 300,000 patients in the United States who have SSc. About a third of the SSc-associated deaths occur because of interstitial lung disease, he added.<\/p>\n<p>Fischer uses a battery of tools, including six-minute walk tests, pulmonary function tests and, most importantly, high-resolution CT imaging to diagnose interstitial lung disease. He uses immunosuppressants, including <a href=\"https:\/\/medicine.umich.edu\/dept\/intmed\/divisions\/rheumatology\/research\/scleroderma-program\/pdf\/Abstracts\/Oral%20Cyclophosphamide%20(CYC)%20and%20Mycophenolate%20Mofitil%20(MMF).pdf\">Cytoxan and CellCept, to treat the 30 percent of SSc patients with progressive interstitial lung disease<\/a>. These are the most serious cases, although all patients with interstitial lung disease must be monitored for evidence of progression.<\/p>\n<p>\u201cThe care of scleroderma patients requires lots of evaluations for potential lung involvement,\u201d Fischer said.<\/p>\n<figure id=\"attachment_14071\" aria-describedby=\"caption-attachment-14071\" style=\"width: 225px\" class=\"wp-caption alignleft\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-14071 size-medium\" src=\"https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050404\/EXT_121917_Joy-and-Granddaughters.jpgsized.webp\" alt=\"A grandmother out in a garden with her granddaughters. One is a baby in diapers. The other is about 4 years old and is looking at some pink flowers.\" width=\"225\" height=\"300\" srcset=\"https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050404\/EXT_121917_Joy-and-Granddaughters.jpgsized.webp 600w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050404\/EXT_121917_Joy-and-Granddaughters.jpgsized-225x300.webp 225w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050404\/EXT_121917_Joy-and-Granddaughters.jpgsized-113x150.webp 113w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050404\/EXT_121917_Joy-and-Granddaughters.jpgsized-200x267.webp 200w\" sizes=\"auto, (max-width: 225px) 100vw, 225px\" \/><figcaption id=\"caption-attachment-14071\" class=\"wp-caption-text\">Joy Mathews with her granddaughters. Mathews was diagnosed with systemic sclerosis four years ago. She battles lung disease and other problems caused by the disease with the help of Dr. Fischer.<\/figcaption><\/figure>\n<p>As a specialist in UCHealth\u2019s <a href=\"https:\/\/www.uchealth.org\/services\/respiratory-lung-care\/comprehensive-lung-breathing-program\/\">Comprehensive Lung and Breathing Program<\/a>, Fischer said he follows several hundred scleroderma patients from Colorado and many states in the Rocky Mountain region and the Pacific Northwest. That includes about 200 new patients each year, he added. The <a href=\"https:\/\/www.scleroderma.org\/site\/SPageServer\/;jsessionid=00000000.app363a?NONCE_TOKEN=D58B5924E58A8C85D24EA4E84B5EFF6C\">Scleroderma Foundation<\/a> cites UCHealth as Colorado\u2019s only center of excellence for treatment of the disease and named Fischer \u201cDoctor of the Year\u201d in 2014.<\/p>\n<h2><strong>Difficult and dangerous opponent<\/strong><\/h2>\n<p>The disease is vexing because it is difficult to recognize and can attack on many fronts and in many ways. For example, thickening and tightening of the skin is a frequent symptom, and a clue to diagnosing the disease. But Fischer noted that SSc does not always affect the skin, and not all patients who have thickened skin have SSc.<\/p>\n<p>In addition, SSc can cause a host of joint, gastrointestinal, kidney and blood vessel problems, such as Raynaud\u2019s phenomenon, which causes arteries to constrict, limiting blood flow, typically to the fingers and toes. Roughly 10 to 15 percent of SSc patients also have pulmonary hypertension, or high blood pressure in the pulmonary artery, which supplies the lungs. It can lead to right-side heart failure. As a result, Fischer works closely with providers in UCH\u2019s Pulmonary Hypertension Clinic.<\/p>\n<p>Simply put, there is no typical SSc patient, Fischer said. \u201cIt\u2019s a complex autoimmune disease that often has varied internal organ involvement that drive prognosis. We need to be on top of where patients are individually.\u201d<\/p>\n<p>The complexity of the disease, he added, also means that \u201cit takes a coordinated, collaborative, interdisciplinary network,\u201d to help evaluate and manage these patients \u2013 which is the design of the Comprehensive Lung and Breathing Program.<\/p>\n<p>For example, nearly all SSc patients have one or more GI problems because the disease scars the smooth muscles of the digestive system, from the esophagus to all regions of the gut, said UCHealth gastroenterologist <a href=\"https:\/\/www.uchealth.org\/provider\/paul-menard-katcher-md\/\">Paul Menard-Katcher, MD<\/a>. While he doesn\u2019t treat the underlying SSc, Menard-Katcher manages a host of symptoms that result from it, including gastroesophageal reflux disease (GERD), diarrhea, and bloating.<\/p>\n<p>\u201cGI manifestations of scleroderma are nearly universal,\u201d Menard-Katcher said. He added that GERD is also implicated in lung disease in SSc patients. That\u2019s because GERD may cause SSc patients to aspirate stomach acids, which can scar the lungs, he said.<\/p>\n<h2><strong>Attack without warning<\/strong><\/h2>\n<p>Joy Mathews of Denver can speak to the mystery and pain of SSc. Mathews, 61, worked in the finance and high-tech industries and earned a PhD from the University of Colorado Boulder in business strategy and entrepreneurship in 2007. With that, she fulfilled a \u201clifelong dream\u201d of teaching, filling a post in Boston for a year, followed by stints at Colorado School of Mines and CU Boulder.<\/p>\n<figure id=\"attachment_14072\" aria-describedby=\"caption-attachment-14072\" style=\"width: 225px\" class=\"wp-caption alignright\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-14072 size-medium\" src=\"https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050438\/EXT_121917_Joy-and-Ele-Copy.jpgsized.webp\" alt=\"Joy, the patient, sits on the ground, reading to her granddaughter, who is about 1-year-old.\" width=\"225\" height=\"300\" srcset=\"https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050438\/EXT_121917_Joy-and-Ele-Copy.jpgsized.webp 600w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050438\/EXT_121917_Joy-and-Ele-Copy.jpgsized-225x300.webp 225w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050438\/EXT_121917_Joy-and-Ele-Copy.jpgsized-113x150.webp 113w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050438\/EXT_121917_Joy-and-Ele-Copy.jpgsized-200x267.webp 200w\" sizes=\"auto, (max-width: 225px) 100vw, 225px\" \/><figcaption id=\"caption-attachment-14072\" class=\"wp-caption-text\">Mathews with granddaughter Elle. The immunosuppressant drugs she takes to treat her lung disease require that Mathews be careful when she is around her grandchildren.<\/figcaption><\/figure>\n<p>But on a trip to Tanzania in November 2013, things began to go wrong, seemingly without warning. Mathews suddenly became \u201cviolently ill,\u201d with severe gastrointestinal problems and joint pain. She felt like her ribs were broken. Not surprisingly, she was \u201ccompletely fatigued\u201d throughout her stay.<\/p>\n<p>After a miserable two weeks she returned to the States, but the illness continued. She lost 25 pounds and was chronically short of breath. Despite the weight loss, her hands were swollen. Physicians in Colorado ran tests, suspecting dengue fever or some other blood-borne disease, but didn\u2019t come up with any answers.<\/p>\n<p>In February 2014, Mathews took matters into her own hands. She flew to the Mayo Clinic in Rochester, Minnesota for tests. Twenty-four hours later, she had a diagnosis: scleroderma. The specialists there also diagnosed her interstitial lung disease. Having an answer gave her a small measure of relief, but her symptoms didn\u2019t improve after she returned to Colorado for care from her rheumatologists.\u00a0They got worse.<\/p>\n<p>Desperate for help, she took another flight, this one to Johns Hopkins Hospital in Baltimore, which has a well-known scleroderma center. The physician she met there told her the biggest issue she had to worry about with scleroderma was her lungs. More surprisingly, she suggested seeing Dr. Aryeh Fischer for her care. Who is Aryeh Fischer, Mathews asked, unaware that a premier physician specializing in her disease was in her own backyard.<\/p>\n<h2><strong>Health at home<\/strong><\/h2>\n<p>In Fischer, Mathews said she found a sympathetic ear \u2013 and more.<\/p>\n<p>\u201cWhen I asked questions, he listened and gave thoughtful answers \u2013 some of which were, \u2018We don\u2019t know.\u2019 With others, he said, \u2018There is something we can do to treat that,\u2019\u201d she said. \u201cI finally understood the things I\u2019d been experiencing.\u201d<\/p>\n<p>Fischer stressed to Mathews that the effects of SSc were not skin-deep.<\/p>\n<p>\u201cThe skin on my face and hands tightened a bit, but no one could look at me and say I had scleroderma based on my skin,\u201d she said. \u201cDr. Fischer understood that my lungs were an issue, that my joints were an issue \u2013 and that\u2019s scleroderma.\u201d<\/p>\n<p>While Mayo had diagnosed her interstitial lung disease, Fischer was the first to explicitly make the link for her between the lung disease and SSc. She knows now from speaking with others who have SSc that there are still many people who don\u2019t know about that connection and continue to think of SSc purely as a skin disease.<\/p>\n<p>Mathews\u2019 problems didn\u2019t disappear after she began seeing Fischer for treatment. For example, he slowed the progression of her lung disease with immunosuppressants and other treatments, allowing her to continue teaching for a time. However, in September 2016, she was getting ready to team-teach a course at CU-Boulder when she fell ill.<\/p>\n<figure id=\"attachment_14070\" aria-describedby=\"caption-attachment-14070\" style=\"width: 300px\" class=\"wp-caption alignleft\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-14070 size-medium\" src=\"https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050317\/EXT_121917_Aryeh-Fischer.jpgsized.webp\" alt=\"Dr. Aryeh Fischer, a UCHealth rheumatologist, sits at his desk.\" width=\"300\" height=\"169\" srcset=\"https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050317\/EXT_121917_Aryeh-Fischer.jpgsized.webp 1200w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050317\/EXT_121917_Aryeh-Fischer.jpgsized-300x169.webp 300w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050317\/EXT_121917_Aryeh-Fischer.jpgsized-1024x576.webp 1024w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050317\/EXT_121917_Aryeh-Fischer.jpgsized-768x432.webp 768w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050317\/EXT_121917_Aryeh-Fischer.jpgsized-150x84.webp 150w, https:\/\/uchealth-wp-uploads.s3.amazonaws.com\/wp-content\/uploads\/sites\/6\/2018\/01\/05050317\/EXT_121917_Aryeh-Fischer.jpgsized-200x113.webp 200w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><figcaption id=\"caption-attachment-14070\" class=\"wp-caption-text\">Dr. Aryeh Fischer, a rheumatologist with UCHealth\u0092&#8217;s Comprehensive Lung and Breathing Program, specializes in treating the interstitial lung disease that often accompanies systemic sclerosis, frequently referred to as scleroderma.<\/figcaption><\/figure>\n<p>She had a blood draw sent to Fischer, who told her to get to the emergency department immediately. It turned out her white blood cell count was so low that she spent a week in isolation at UCH and went home with a mask to prevent infection. It turned out she had had a rare reaction to one of the medications for her SSc. Mathews reluctantly concluded the uncertainty of dealing with SSc meant she couldn\u2019t live up to her commitment to teach, and she has not returned to the classroom.<\/p>\n<p>Things had improved at the beginning of 2017, but then her lung disease worsened, requiring her to get chemotherapy infusions every four weeks, with a second treatment every six months.<\/p>\n<p>\u201cThat was pretty miserable,\u201d Mathews said. Fischer prescribed oral medications as an alternative, but after a couple of months of difficult side effects, including severe fatigue, he discontinued chemotherapy for a month to improve her quality of life. He\u2019s now considering alternative treatments.<\/p>\n<p>The biggest benefit of that decision: Getting off immunosuppressants means that Mathews will be able to enjoy her three granddaughters \u2013 including the last one, born Dec. 1 &#8211; in the new year.<\/p>\n<h2><strong>Attack on multiple fronts<\/strong><\/h2>\n<p>The battle isn\u2019t confined to her lungs. A rare reaction to CellCept caused a bout with colitis that Fischer treated with medications. He prescribes a different chemotherapy infusion that helps ease her joint pain. Menard-Katcher works with Fischer to help Mathews manage her GI issues.<\/p>\n<p>The ordeal has changed her life. The uncertainty of SSc not only means that she can\u2019t teach, but also that she can\u2019t always travel with her husband. The physical toll is enormous \u2013 something that isn\u2019t readily apparent to others.<\/p>\n<p>\u201cPeople like me who don\u2019t have a skin impact can walk out of the house and people think, \u2018She\u2019s healthy,\u2019\u201d Mathews said. \u201cYou don\u2019t look ill particularly, but you know something is wrong. And people don\u2019t understand what the fatigue is. It\u2019s not just tired, it\u2019s all day long. You can lie down, but you\u2019re just exhausted.\u201d<\/p>\n<p>But Mathews has not succumbed to SSc. Rather, she fights back. She does pulmonary rehabilitation and has even begun swimming again, with the help of a floating beer cooler to protect her oxygen tank and tubing.<\/p>\n<p>\u201cIt\u2019s wonderful to swim again,\u201d she said.<\/p>\n<p>For his part, Fischer acknowledges that treating SSc has historically been a source of pessimism for providers and patients. But clinical trials of medications, research into biomarkers for the disease, and investigations of possible risk factors give him hope for the future.<\/p>\n<p>\u201cI\u2019m not here to be falsely optimistic, but we can help people ease their suffering and navigate a tough illness,\u201d he said. \u201cThat takes a village.\u201d<\/p>\n<p>Four years after her diagnosis, Mathews can also finally offer a note of optimism. \u201cI feel light years better because of Dr. Fischer and I know he will treat any scleroderma \u2018surprises\u2019 in the future.\u201d<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Dr. Aryeh Fischer is a rheumatologist who is an expert in diagnosing and treating lung disease in patients with a condition that is too often associated only with the skin. If that sounds confusing, it\u2019s befitting of an autoimmune disorder that is not only rare and elusive but even misleadingly named: scleroderma. Its Greek origins [&hellip;]<\/p>\n","protected":false},"author":2143,"featured_media":14073,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","footnotes":""},"categories":[5],"tags":[2597,3357,177],"class_list":["post-14062","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-innovative-care","tag-comprehensive-lung-and-breathing-program","tag-lung-and-respiratory-care-pulmonology","tag-pulmonology"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.2 (Yoast SEO v27.2) - 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