Effective treatment of malignant atrophic papulosis (Köhlmeier-Degos disease) with treprostinil – early experience

Patient one is a now 42-year-old woman initially seen in 2008. She presented then with a three year history of cold-induced blanching of her hands and feet, retrosternal heartburn of similar duration, with esophageal dysmotility on barium swallow. Anti-nuclear antibody (ANA) was present at a titer of 1:640 in anti-nucleolar pattern. Anti-topoisomerase antibody, anti-U1 RNP antibody, SS-A, and SS-B antibodies were negative.

In the year prior to her presentation, she developed alopecia, lymphadenopathy, and autoimmune hemolytic anemia. Bone marrow demonstrated hypercellular marrow with polyclonal T-cell lymphocytes, mild dyserythropoiesis, and dysgranulopoiesis. She was placed on prednisone and mycophenolate. When seen, she had 1+ digital and facial skin thickening on a Rodnan skin score of 0 to 3+. She also presented with extensive avascular lesions with telangiectatic borders at her digits and hands, upper arms, chest, and toes (Additional files1,2,3). Skin biopsy of upper arm lesion was initially read as “consistent with lupus”. Proton pump inhibitor and hydroxychloroquine were added to her drug regimen. The skin lesions increased in extent and chloroquine was substituted for hydroxychloroquine without benefit. In early 2009, she developed pericarditis and pericardial tamponade and had a pericardial window placed. She also required cholecystectomy because of gangrenous cholecystitis. Cardiac catheterization post surgery demonstrated mean pulmonary artery (PA) pressure of 32/10. She experienced a grand mal seizure and was placed on Keppra. Mycophenolate was withdrawn and she received monthly pulse cyclophosphamide for six months and then was placed on azathioprine. Profound hypocomplementemia resolved, anti-DNA antibody, previously modestly elevated, disappeared.

She developed progressive dyspnea and in early 2010 on echocardiogram revealed estimated PA systolic pressure of 58. Right heart catheterization demonstrated mean PA pressure of 36.

Skin lesions, resembling clinically and histologically those of MAP, continued to increase in number. She also was experiencing frequent abdominal pain. Laparoscopy was performed but no serosal lesion suggestive of MAP was seen and her abdominal pain spontaneously abated. Therapy with subcutaneous treprostinil was initiated in August 2010 and titrated over a few months to 38.75 ng/kg/min. Within a month, she noted improved functional status with less dyspnea. She reported less discomfort at her hands and toes (she had been requiring fentanyl 75 mcg patches and hydromorphone 2 mg 2–3 times per day). Within three months of initiating therapy, she noted that the digital lesions were diminishing in size and the lesions on her upper arms and inframammary areas showed marked involution. No new lesion developed. Her World Health Organization (WHO) functional status improved to class II. She had sustained improvement so that by six months of therapy, the digital lesions more or less completely resolved and the toe lesions resolved soon thereafter. Residual scarring has persisted at the upper arms and inframammary area (Additional files1,2,3). She has had no new neurologic event or any recurrence of abdominal pain.

Patient two, a 17-year-old male, was first seen in our clinic in August 2009. He had a two year history of an increasing number of avascular slightly depressed porcelain like lesions with an erythematous rim, primarily on his chest and abdomen, with more scattered lesions on his limbs, but none on his head, back or genitalia. Biopsy of a truncal lesion was consistent with a diagnosis of MAP (Additional file4). He had no clinical or serologic findings to suggest overlap with any connective tissue disorder. Colonoscopy revealed a limited number of similar appearing lesions on the bowel wall. Within a few months, he started to experience episodes of crampy abdominal pain. These increased in frequency and intensity and he developed an acute abdomen in December 2009. At laparotomy, the serosa of the small bowel revealed hundreds of lesions consistent with MAP (Additional file5). He had peritoneal fluid with polymicrobial growth but no area of bowel perforation was identified. He was treated with broad spectrum antibiotic therapy but redeveloped evidence of acute abdomen and required re-exploration 10 days later. He was found to have edematous and ischemic appearing loops of bowl with “abdominal compartment syndrome;” but again, no frank perforation. The abdominal wound was left open. He remained febrile, hypertensive, and tachycardic. He was treated with IV eculizumab based on successful use of this agent in a patient similarly afflicted[9‐11]. Almost immediate improvement was noted, with resolution of fever and tachycardia and a decrease in swelling of the bowel loops. On continued eculizumab, he had sustained improvement and the abdominal wound was successfully closed after another 10 days.

He was able to return to school within two months without abdominal pain.

Despite continued eculizumab therapy, by late 2010 he had redeveloped bouts of abdominal pain and he had developed gross hematuria with cystoscopy showing lesions suspicious for MAP. The abdominal pain was of such severity as to require bowel rest and parenteral nutrition. Eculizumab dose was increased at this time hoping for better tissue penetration. Peak and trough levels of eculizumab were adequate to assure complete suppression of C5 activation. He also developed evidence of CNS disease with intermittent episodes of aphasia and arm numbness with new abnormalities on MRI consistent with findings described in other individuals with MAP (Additional file6). At this point, the frequency of eculizumab was increased.

Based on our experience with patient one, who by this time had shown clearing of most of her skin lesions, we were able to obtain approval for subcutaneous treprostinil therapy on a compassionate use basis and it was initiated on December 28, 2010 and titrated upwards.

Due to continued abdominal pain, on January 24, 2011, he underwent laparoscopic surgery. Multiple adhesions were identified and lysed, but all previously noted serosal lesions of MAP had resolved (the surgeon was the same surgeon who had operated upon him in 2009.) Since that time, he has had no further abdominal pain and has gained weight progressively. He noted gradual involution of skin lesions, although these responded less rapidly and dramatically than those in patient one. He has had no further CNS event and repeated MRI showed improvement (Additional file6). At last examination he had no neurologic deficit. He had no further gross or microscopic hematuria. Repeat cystoscopy was not performed. His current treprostinil dose is 32 ng/kg/min. He is attending college full-time and working in a supermarket part-time.